Canonical Allele Identifier: CA1373414354
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965114G= , CM000665.2:g.69965114G= GRCh38
NC_000003.11:g.70014265G= , CM000665.1:g.70014265G= GRCh37
NC_000003.10:g.70096955G= NCBI36
NG_011631.1:g.230633G= , LRG_776:g.230633G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1381G= ENSP00000324443.5:p.Asp461=
ENST00000687384.1:c.1378G= ENSP00000510225.1:p.Asp460=
ENST00000689390.1:n.1603G=
ENST00000693031.1:c.1354G= ENSP00000509845.1:p.Asp452=
ENST00000693549.1:c.*192G= ENSP00000509358.1:n.*192G=
ENST00000314589.10:c.1381G= ENSP00000324443.5:p.Asp461=
ENST00000352241.9:c.1447G= MANE Select ENSP00000295600.8:p.Asp483=
ENST00000394351.9:c.1126G= MANE Plus Clinical ENSP00000377880.3:p.Asp376=
ENST00000448226.9:c.1426G= ENSP00000391803.3:p.Asp476=
ENST00000642352.1:c.1429G= ENSP00000494105.1:p.Asp477=
ENST00000314557.10:c.1108G= ENSP00000324246.6:p.Asp370=
ENST00000314589.9:c.1381G= ENSP00000324443.5:p.Asp461=
ENST00000328528.10:c.1426G= ENSP00000327867.6:p.Asp476=
ENST00000352241.8:c.1429G= ENSP00000295600.7:p.Asp477=
ENST00000394351.7:c.1126G= ENSP00000377880.3:p.Asp376=
ENST00000448226.6:c.1447G= ENSP00000391803.2:p.Asp483=
ENST00000472437.5:c.1273G= ENSP00000418845.1:p.Asp425=
ENST00000478490.5:c.*773G= ENSP00000433487.1:n.*773G=
ENST00000531774.1:c.940G= ENSP00000435909.1:p.Asp314=
NM_000248.3:c.1126G= , LRG_776t1:c.1126G= NP_000239.1:p.Asp376=
NM_001184967.1:c.1273G= NP_001171896.1:p.Asp425=
NM_006722.2:c.1426G= NP_006713.1:p.Asp476=
NM_198158.2:c.1108G= NP_937801.1:p.Asp370=
NM_198159.2:c.1429G= NP_937802.1:p.Asp477=
NM_198177.2:c.1381G= NP_937820.1:p.Asp461=
NM_198178.2:c.940G= NP_937821.2:p.Asp314=
XM_005264754.1:c.1447G= XP_005264811.1:p.Asp483=
XM_005264755.2:c.1399G= XP_005264812.1:p.Asp467=
XM_006713164.2:c.1291G= XP_006713227.1:p.Asp431=
XM_011533722.1:c.1444G= XP_011532024.1:p.Asp482=
XM_011533723.1:c.1396G= XP_011532025.1:p.Asp466=
XM_011533724.1:c.1291G= XP_011532026.1:p.Asp431=
XM_011533725.1:c.1279G= XP_011532027.1:p.Asp427=
XM_011533726.1:c.1261G= XP_011532028.1:p.Asp421=
NM_001354604.1:c.1447G= NP_001341533.1:p.Asp483=
NM_001354605.1:c.1444G= NP_001341534.1:p.Asp482=
NM_001354606.1:c.1426G= NP_001341535.1:p.Asp476=
NM_001354607.1:c.1378G= NP_001341536.1:p.Asp460=
NM_001354608.1:c.1273G= NP_001341537.1:p.Asp425=
NM_001184967.2:c.1273G= NP_001171896.1:p.Asp425=
NM_001354604.2:c.1447G= MANE Select NP_001341533.1:p.Asp483=
NM_001354605.2:c.1444G= NP_001341534.1:p.Asp482=
NM_001354606.2:c.1426G= NP_001341535.1:p.Asp476=
NM_001354607.2:c.1378G= NP_001341536.1:p.Asp460=
NM_001354608.2:c.1273G= NP_001341537.1:p.Asp425=
NM_198158.3:c.1108G= NP_937801.1:p.Asp370=
NM_198159.3:c.1429G= NP_937802.1:p.Asp477=
NM_198177.3:c.1381G= NP_937820.1:p.Asp461=
NM_198178.3:c.940G= NP_937821.2:p.Asp314=
NM_000248.4:c.1126G= MANE Plus Clinical NP_000239.1:p.Asp376=
NM_006722.3:c.1426G= NP_006713.1:p.Asp476=