Transcript #00026048 (NM_001377265.1, MAPT gene)

Transcript name transcript variant 9 (removed from reference sequence) (removed from reference sequence) (removed from reference sequence)
Gene name MAPT (microtubule-associated protein tau)
Chromosome 17
Transcript - NCBI ID NM_001377265.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001364194.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2026-02-12 15:19:58 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.*2167G>A r.(?) p.(=)
-/. - c.*26T>C r.(?) p.(=)
?/. - c.*64G>A r.(?) p.(=)
?/. - c.*68_*70del r.(?) p.(=)
-/. - c.-13A>G r.(?) p.(=)
-/. - c.-13A>G r.(?) p.(=)
-/. - c.-13A>G r.(?) p.(=)
+/+ - c.14G>A r.(?) p.(Arg5His)
+/+ - c.14G>T r.(?) p.(Arg5Leu)
-/? - c.42C>T r.(?) p.(His14=)
-/? - c.50C>T r.(?) p.(Thr17Met)
-/? - c.54C>T r.(?) p.(Tyr18=)
?/. - c.55G>T r.(?) p.(Gly19Trp)
-/? - c.88A>G r.(?) p.(Thr30Ala)
-/? - c.117G>A r.(?) p.(Thr39=)
?/. - c.121G>A r.(?) p.(Ala41Thr)
-?/. - c.134-2537T>C r.(?) p.(=)
+/. - c.163G>A r.(?) p.(Gly55Arg)
?/. - c.176C>T r.(?) p.(Pro59Leu)
-/. - c.220+18C>T r.(?) p.(=)
-/. - c.220+18C>T r.(?) p.(=)
-/. - c.220+18C>T r.(?) p.(=)
-?/. - c.220+2432G>A r.(?) p.(=)
-/. - c.220+2432G>A r.(?) p.(=)
-?/. - c.220+2475G>A r.(?) p.(=)
-/- - c.220+2475G>A r.(?) p.(=)
-?/. - c.220+2477C>G r.(?) p.(=)
-?/. - c.220+2477C>G r.(?) p.(=)
?/. - c.220+2503C>T r.(?) p.(=)
-?/. - c.220+2503C>T r.(?) p.(=)
-/. - c.220+2535A>G r.(?) p.(=)
-/. - c.220+2535A>G r.(?) p.(=)
-/. - c.220+2535A>G r.(?) p.(=)
-/. - c.220+2535A>G r.(?) p.(=)
-?/. - c.220+2538C>G r.(?) p.(=)
-?/. - c.220+2538C>G r.(?) p.(=)
?/. - c.232G>A r.(?) p.(Gly78Ser)
-/. - c.547G>A r.(?) p.(Glu183Lys)
-?/. - c.629G>T r.(?) p.(Gly210Val)
?/. - c.643C>T r.(?) p.(Pro215Ser)
+/. - c.653dup r.(?) p.(Gly219ArgfsTer18)
-?/. - c.660G>C r.(?) p.(Leu220=)
?/. - c.727C>T r.(?) p.(Arg243Cys)
-/? - c.830C>T r.(?) p.(Pro277Leu)
-/. - c.830C>T r.(?) p.(Pro277Leu)
-/. - c.830C>T r.(?) p.(Pro277Leu)
-?/. - c.841G>A r.(?) p.(Ala281Thr)
-?/. - c.862G>A r.(?) p.(Gly288Arg)
-?/. - c.862G>A r.(?) p.(Gly288Arg)
-?/. - c.889C>A r.(?) p.(Arg297Ser)
-?/. - c.889C>A r.(?) p.(Arg297Ser)
?/. - c.896T>G r.(?) p.(Val299Gly)
?/. - c.896T>G r.(?) p.(Val299Gly)
-?/. - c.896T>G r.(?) p.(Val299Gly)
-?/. - c.896T>G r.(?) p.(Val299Gly)
-?/. - c.912C>A r.(?) p.(Pro304=)
-/? - c.914A>G r.(?) p.(Gln305Arg)
-/. - c.914A>G r.(?) p.(Gln305Arg)
-/. - c.914A>G r.(?) p.(Gln305Arg)
-/. - c.914A>G r.(?) p.(Gln305Arg)
-/. - c.914A>G r.(?) p.(Gln305Arg)
-/. - c.914A>G r.(?) p.(Gln305Arg)
-?/. - c.1008G>A r.(?) p.(Ala336=)
?/. - c.1028C>G r.(?) p.(Pro343Arg)
-/? - c.1078G>A r.(?) p.(Asp360Asn)
-/. - c.1078G>A r.(?) p.(Asp360Asn)
-/. - c.1078G>A r.(?) p.(Asp360Asn)
-/? - c.1080C>T r.(?) p.(Asp360=)
-/. - c.1080C>T r.(?) p.(Asp360=)
-/. - c.1080C>T r.(?) p.(Asp360=)
-/? - c.1091T>C r.(?) p.(Val364Ala)
-/. - c.1091T>C r.(?) p.(Val364Ala)
-/. - c.1091T>C r.(?) p.(Val364Ala)
-?/. - c.1115C>T r.(?) p.(Ala372Val)
?/. - c.1144A>G r.(?) p.(Ile382Val)
-/. - c.1178C>T r.(?) p.(Ser393Leu)
-?/. - c.1178C>T r.(?) p.(Ser393Leu)
-?/. - c.1240G>A r.(?) p.(Gly414Ser)
?/. - c.1307C>T r.(?) p.(Ala436Val)
-?/. - c.1326C>T r.(?) p.(Pro442=)
-?/. - c.1326C>T r.(?) p.(Pro442=)
-/? - c.1333C>T r.(?) p.(Arg445Trp)
-/. - c.1333C>T r.(?) p.(Arg445Trp)
-/. - c.1333C>T r.(?) p.(Arg445Trp)
-?/. - c.1351+21C>T r.(?) p.(=)
-?/. - c.1359G>C r.(?) p.(Met453Ile)
?/. - c.1366A>G r.(?) p.(Lys456Glu)
-?/. - c.1389C>T r.(?) p.(Ser463=)
-?/. - c.1443T>C r.(?) p.(Asn481=)
?/. - c.1505C>T r.(?) p.(Ser502Phe)
-?/. - c.1505C>T r.(?) p.(Ser502Phe)
?/. - c.1505C>T r.(?) p.(Ser502Phe)
-/. - c.1546T>C r.(?) p.(Tyr516His)
-/. - c.1546T>C r.(?) p.(Tyr516His)
-/. - c.1546T>C r.(?) p.(Tyr516His)
-/. - c.1546T>C r.(?) p.(Tyr516His)
-/? - c.1564T>C r.(?) p.(Ser522Pro)
-/. - c.1564T>C r.(?) p.(Ser522Pro)
-/. - c.1564T>C r.(?) p.(Ser522Pro)
-/. - c.1564T>C r.(?) p.(Ser522Pro)
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