Transcript #00025774 (NM_002294.2, LAMP2 gene)

Transcript name transcript variant A
Gene name LAMP2 (lysosomal-associated membrane protein 2)
Chromosome X
Transcript - NCBI ID NM_002294.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002285.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-12-18 12:32:33 +01:00 (CET)
Date last edited N/A


Variants

277 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-24880_65-3489del r.(=) p.(=)
+/. _1_9_ c.-180_*5175del r.0 p.0
+/. _1_9_ c.-180_*5175del r.0 p.0
+?/. - c.-39_-31del r.(=) p.(=)
-/. - c.-23_-15del r.(?) p.(=)
-/. - c.-23_-15del r.(?) p.(=)
-/. - c.-23_-15del r.(?) p.(=)
-/. - c.-23_-15dup r.(?) p.(=)
-/. - c.-4G>C r.(?) p.(=)
-?/. - c.-4G>C r.(?) p.(=)
?/. - c.4G>C r.(?) p.(Val2Leu)
-?/. - c.9C>T r.(?) p.(Cys3=)
-?/. - c.9C>T r.(?) p.(Cys3=)
?/. - c.10T>C r.(?) p.(Phe4Leu)
+/. - c.14del r.(?) p.(Arg5Profs*15)
+/. - c.30_36del r.(?) p.(Gly13Phefs*5)
-?/. - c.42C>T r.(?) p.(Leu14=)
-/. - c.42C>T r.(?) p.(Leu14=)
-?/. - c.42C>T r.(?) p.(Leu14=)
-?/. - c.49G>A r.(?) p.(Val17Ile)
+/. - c.56T>G r.(?) p.(Leu19Arg)
+/. - c.64+1G>A r.spl? p.?
+/. - c.64+1G>A r.spl? p.?
+/. - c.64+1G>T r.spl? p.?
-/. - c.64+11G>C r.(=) p.(=)
-?/. - c.65-20A>T r.(=) p.(=)
-/. - c.65-20_65-18del r.(=) p.(=)
-?/. - c.65-13T>A r.(=) p.(=)
+/. - c.65-2A>G r.spl? p.?
+?/+? - c.65-2A>G r.spl? p.?
?/. - c.73C>T r.(?) p.(Arg25Trp)
?/. - c.73C>T r.(?) p.(Arg25Trp)
-/. - c.74G>A r.(?) p.(Arg25Gln)
-?/. - c.74G>A r.(?) p.(Arg25Gln)
-?/. - c.85T>C r.(?) p.(Leu29=)
-/. - c.85T>C r.(?) p.(Leu29=)
+/. - c.102_103del r.(?) p.(Asp35Phefs*20)
?/. - c.112A>T r.(?) p.(Asn38Tyr)
-?/. - c.115_118del r.(?) p.(Ala39LeufsTer9)
+/. - c.127del r.(?) p.(Tyr43MetfsTer6)
+/. - c.137G>A r.(?) p.(Trp46*)
+/. - c.138G>A r.(?) p.(Trp46*)
-/. - c.156A>T r.(?) p.(Val52=)
-/. - c.156A>T r.(=) p.(=)
?/. - c.156A>T r.(=) p.(=)
-/. - c.156A>T r.(=) p.(=)
-/. - c.156A>T r.(=) p.(=)
-?/. - c.156A>T r.(=) p.(=)
-?/. - c.156A>T r.(=) p.(=)
-/. - c.156A>T r.(?) p.(Val52=)
-?/. - c.157C>T r.(?) p.(Arg53Cys)
-?/. - c.157C>T r.(?) p.(Arg53Cys)
-?/. - c.157C>T r.(?) p.(Arg53Cys)
?/. - c.166A>G r.(?) p.(Thr56Ala)
+/. - c.179del r.(?) p.(Thr60Ilefs*5)
+/. - c.183+1G>A r.spl? p.?
+?/. - c.183+5G>A r.spl? p.?
?/. - c.183+9A>G r.(=) p.(=)
+/. - c.184-1_189del r.? p.?
?/. - c.188C>T r.(?) p.(Thr63Ile)
-/. - c.188C>T r.(?) p.(Thr63Ile)
?/. - c.188C>T r.(?) p.(Thr63Ile)
?/. - c.188C>T r.(?) p.(Thr63Ile)
+/. - c.189_190del r.(?) p.(Val64Asnfs*11)
+/. - c.205del r.(?) p.(His69Metfs*4)
-?/. - c.209G>T r.(?) p.(Gly70Val)
-/. - c.213T>C r.(?) p.(Thr71=)
+/. - c.238del r.(?) p.(Asp81Metfs*8)
+?/. - c.239G>T r.(?) p.(Gly80Val)
+/. - c.247C>T r.(?) p.(Gln83*)
+/. - c.247C>T r.(?) p.(Gln83*)
+/. - c.256_257del r.(?) p.(Pro86Glnfs*26)
-?/. - c.267A>C r.(?) p.(Ala89=)
?/. - c.269T>A r.(?) p.(Val90Glu)
+/. - c.286_287del r.(?) p.(Ser97Leufs*15)
+/. - c.293G>A r.(?) p.(Trp98*)
+/. - c.294G>A r.(?) p.(Trp98*)
+/. - c.294G>A r.(?) p.(Trp98*)
+/. - c.294G>A r.(?) p.(Trp98*)
?/. - c.299C>T r.(?) p.(Ala100Val)
+/. - c.317_320dup r.(?) p.(Thr108Ilefs*6)
+/. - c.327T>A r.(?) p.(Tyr109*)
-?/. - c.339C>T r.(?) p.(Ser113=)
-?/. - c.339C>T r.(?) p.(Ser113=)
-/. - c.339C>T r.(?) p.(Ser113=)
-?/. - c.339C>T r.(?) p.(Ser113=)
-?/. - c.339C>T r.(?) p.(Ser113=)
?/. - c.358A>G r.(?) p.(Thr120Ala)
-?/. - c.358A>G r.(?) p.(Thr120Ala)
-/. - c.372A>G r.(?) p.(Thr124=)
?/. - c.373_375del r.(?) p.(Thr125del)
-?/. - c.385G>A r.(?) p.(Ala129Thr)
-/. - c.385G>A r.(?) p.(Ala129Thr)
-/. - c.397+16del r.(=) p.(=)
+/. - c.397+1801_741+688dup r.? p.?
?/. - c.398-5del r.spl? p.?
-?/. - c.398-5T>C r.spl? p.?
-?/. - c.398-5T>C r.spl? p.?
-?/. - c.398-4A>G r.spl? p.?
+/. - c.(?_398)_(*355314_?)del r.? p.?
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