Transcript #00002264 (NM_138420.2, AHNAK2 gene)

Transcript name AHNAK nucleoprotein 2
Gene name AHNAK2 (AHNAK nucleoprotein 2)
Chromosome 14
Transcript - NCBI ID NM_138420.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_612429.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

342 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.114T>C r.(?) p.(Ser38=)
-?/. - c.156G>A r.(?) p.(Pro52=)
?/. - c.167C>T r.(?) p.(Ser56Leu)
-?/. - c.288G>C r.(?) p.(Arg96=)
-?/. - c.412G>A r.(?) p.(Val138Ile)
-?/. - c.442G>A r.(?) p.(Ala148Thr)
-?/. - c.652-9_652-8del r.(=) p.(=)
-?/. - c.695C>T r.(?) p.(Thr232Ile)
?/. - c.811C>T r.(?) p.(Arg271Trp)
-?/. - c.1055G>A r.(?) p.(Arg352His)
?/. - c.1127G>A r.(?) p.(Arg376Lys)
-?/. - c.1127G>T r.(?) p.(Arg376Met)
-?/. - c.1198G>A r.(?) p.(Gly400Ser)
-?/. - c.1198G>A r.(?) p.(Gly400Ser)
-?/. - c.1215C>T r.(?) p.(Cys405=)
-/. - c.1254G>T r.(?) p.(Arg418Ser)
?/. - c.1462G>A r.(?) p.(Asp488Asn)
-?/. - c.1462G>A r.(?) p.(Asp488Asn)
-?/. - c.1522C>T r.(?) p.(Leu508Phe)
-?/. - c.1538G>A r.(?) p.(Arg513Gln)
?/. - c.1675G>T r.(?) p.(Gly559*)
-?/. - c.1699G>A r.(?) p.(Glu567Lys)
-?/. - c.1713G>A r.(?) p.(Lys571=)
-?/. - c.1732G>A r.(?) p.(Gly578Arg)
-?/. - c.1967G>T r.(?) p.(Arg656Leu)
?/. - c.2005G>A r.(?) p.(Ala669Thr)
-?/. - c.2091G>A r.(?) p.(Ser697=)
?/. - c.2315A>G r.(?) p.(Asp772Gly)
?/. - c.2384C>T r.(?) p.(Ser795Phe)
?/. - c.2417C>T r.(?) p.(Pro806Leu)
-?/. - c.2435G>C r.(?) p.(Gly812Ala)
-?/. - c.2458T>C r.(?) p.(Ser820Pro)
-?/. - c.2466C>T r.(?) p.(Ala822=)
-?/. - c.2475G>T r.(?) p.(Glu825Asp)
?/. - c.2562C>G r.(?) p.(Asp854Glu)
-?/. - c.2632G>A r.(?) p.(Ala878Thr)
?/. - c.2778G>A r.(?) p.(Met926Ile)
?/. - c.2782A>G r.(?) p.(Lys928Glu)
-?/. - c.2970C>T r.(?) p.(Asp990=)
-?/. - c.3081G>A r.(?) p.(=)
-?/. - c.3094C>A r.(?) p.(Leu1032Met)
-?/. - c.3094C>G r.(?) p.(Leu1032Val)
-?/. - c.3145C>G r.(?) p.(Gln1049Glu)
-?/. - c.3259C>G r.(?) p.(Pro1087Ala)
-/. - c.3407C>T r.(?) p.(Pro1136Leu)
?/. - c.3428C>T r.(?) p.(Ala1143Val)
-?/. - c.3451C>T r.(?) p.(Leu1151=)
-?/. - c.3465T>C r.(?) p.(Asp1155=)
-?/. - c.3485G>A r.(?) p.(Arg1162Lys)
-?/. - c.3495G>T r.(?) p.(Met1165Ile)
-?/. - c.3501G>A r.(?) p.(Lys1167=)
-/. - c.3513A>C r.(?) p.(Pro1171=)
-/. - c.3516G>C r.(?) p.(Ser1172=)
-?/. - c.3521G>T r.(?) p.(Gly1174Val)
-?/. - c.3525G>A r.(?) p.(Ala1175=)
-?/. - c.3555G>A r.(?) p.(Ser1185=)
-?/. - c.3557T>C r.(?) p.(Val1186Ala)
-?/. - c.3557T>C r.(?) p.(Val1186Ala)
-?/. - c.3566C>G r.(?) p.(Ser1189Cys)
-?/. - c.3590T>G r.(?) p.(Val1197Gly)
-?/. - c.3598C>T r.(?) p.(Pro1200Ser)
-?/. - c.3612G>A r.(?) p.(Gly1204=)
-?/. - c.3667C>T r.(?) p.(His1223Tyr)
-?/. - c.3673G>A r.(?) p.(Gly1225Ser)
-?/. - c.3922G>A r.(?) p.(Ala1308Thr)
-?/. - c.4121C>T r.(?) p.(Thr1374Ile)
-?/. - c.4237A>C r.(?) p.(Lys1413Gln)
?/. - c.4336G>C r.(?) p.(Glu1446Gln)
-?/. - c.4485G>T r.(?) p.(Met1495Ile)
-?/. - c.4514T>C r.(?) p.(Val1505Ala)
-?/. - c.4515G>A r.(?) p.(Val1505=)
-?/. - c.4518T>A r.(?) p.(Ser1506=)
-?/. - c.4527C>G r.(?) p.(Gly1509=)
-?/. - c.4537G>A r.(?) p.(Glu1513Lys)
-?/. - c.4541C>T r.(?) p.(Ala1514Val)
-?/. - c.4544C>T r.(?) p.(Ser1515Leu)
-?/. - c.4547T>C r.(?) p.(Val1516Ala)
-?/. - c.4572G>A r.(?) p.(Glu1524=)
-?/. - c.4583G>T r.(?) p.(Ser1528Ile)
-?/. - c.4637C>T r.(?) p.(Pro1546Leu)
-?/. - c.4644T>C r.(?) p.(Ala1548=)
-?/. - c.4648C>G r.(?) p.(Leu1550Val)
-?/. - c.4651G>A r.(?) p.(Glu1551Lys)
-?/. - c.4659G>C r.(?) p.(Gln1553His)
-?/. - c.4668A>C r.(?) p.(Gln1556His)
?/. - c.4668A>G r.(?) p.(Gln1556=)
-?/. - c.4694C>A r.(?) p.(Pro1565His)
-?/. - c.4695T>G r.(?) p.(Pro1565=)
-?/. - c.4779G>C r.(?) p.(Gly1593=)
-?/. - c.4786A>C r.(?) p.(Ile1596Leu)
?/. - c.4970A>G r.(?) p.(Lys1657Arg)
-?/. - c.5025G>C r.(?) p.(Lys1675Asn)
-?/. - c.5031C>T r.(?) p.(Ile1677=)
?/. - c.5033A>C r.(?) p.(Glu1678Ala)
-?/. - c.5036C>A r.(?) p.(Ala1679Asp)
-?/. - c.5083C>T r.(?) p.(Pro1695Ser)
-?/. - c.5090T>C r.(?) p.(Met1697Thr)
-?/. - c.5116C>A r.(?) p.(Leu1706Ile)
-?/. - c.5119A>T r.(?) p.(Ser1707Cys)
-?/. - c.5128T>C r.(?) p.(Ser1710Pro)
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