Canonical Allele Identifier: CA1373413950
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69964908C= , CM000665.2:g.69964908C= GRCh38
NC_000003.11:g.70014059C= , CM000665.1:g.70014059C= GRCh37
NC_000003.10:g.70096749C= NCBI36
NG_011631.1:g.230427C= , LRG_776:g.230427C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1175C= ENSP00000324443.5:p.Ser392=
ENST00000687384.1:c.1172C= ENSP00000510225.1:p.Ser391=
ENST00000689390.1:n.1397C=
ENST00000693031.1:c.1148C= ENSP00000509845.1:p.Ser383=
ENST00000693549.1:c.1114-6C= ENSP00000509358.1:n.1114-6C=
ENST00000314589.10:c.1175C= ENSP00000324443.5:p.Ser392=
ENST00000352241.9:c.1241C= MANE Select ENSP00000295600.8:p.Ser414=
ENST00000394351.9:c.920C= MANE Plus Clinical ENSP00000377880.3:p.Ser307=
ENST00000448226.9:c.1220C= ENSP00000391803.3:p.Ser407=
ENST00000642352.1:c.1223C= ENSP00000494105.1:p.Ser408=
ENST00000314557.10:c.902C= ENSP00000324246.6:p.Ser301=
ENST00000314589.9:c.1175C= ENSP00000324443.5:p.Ser392=
ENST00000328528.10:c.1220C= ENSP00000327867.6:p.Ser407=
ENST00000352241.8:c.1223C= ENSP00000295600.7:p.Ser408=
ENST00000394351.7:c.920C= ENSP00000377880.3:p.Ser307=
ENST00000448226.6:c.1241C= ENSP00000391803.2:p.Ser414=
ENST00000472437.5:c.1067C= ENSP00000418845.1:p.Ser356=
ENST00000478490.5:c.*567C= ENSP00000433487.1:n.*567C=
ENST00000531774.1:c.734C= ENSP00000435909.1:p.Ser245=
NM_000248.3:c.920C= , LRG_776t1:c.920C= NP_000239.1:p.Ser307=
NM_001184967.1:c.1067C= NP_001171896.1:p.Ser356=
NM_006722.2:c.1220C= NP_006713.1:p.Ser407=
NM_198158.2:c.902C= NP_937801.1:p.Ser301=
NM_198159.2:c.1223C= NP_937802.1:p.Ser408=
NM_198177.2:c.1175C= NP_937820.1:p.Ser392=
NM_198178.2:c.734C= NP_937821.2:p.Ser245=
XM_005264754.1:c.1241C= XP_005264811.1:p.Ser414=
XM_005264755.2:c.1193C= XP_005264812.1:p.Ser398=
XM_006713164.2:c.1085C= XP_006713227.1:p.Ser362=
XM_011533722.1:c.1238C= XP_011532024.1:p.Ser413=
XM_011533723.1:c.1190C= XP_011532025.1:p.Ser397=
XM_011533724.1:c.1085C= XP_011532026.1:p.Ser362=
XM_011533725.1:c.1073C= XP_011532027.1:p.Ser358=
XM_011533726.1:c.1055C= XP_011532028.1:p.Ser352=
NM_001354604.1:c.1241C= NP_001341533.1:p.Ser414=
NM_001354605.1:c.1238C= NP_001341534.1:p.Ser413=
NM_001354606.1:c.1220C= NP_001341535.1:p.Ser407=
NM_001354607.1:c.1172C= NP_001341536.1:p.Ser391=
NM_001354608.1:c.1067C= NP_001341537.1:p.Ser356=
NM_001184967.2:c.1067C= NP_001171896.1:p.Ser356=
NM_001354604.2:c.1241C= MANE Select NP_001341533.1:p.Ser414=
NM_001354605.2:c.1238C= NP_001341534.1:p.Ser413=
NM_001354606.2:c.1220C= NP_001341535.1:p.Ser407=
NM_001354607.2:c.1172C= NP_001341536.1:p.Ser391=
NM_001354608.2:c.1067C= NP_001341537.1:p.Ser356=
NM_198158.3:c.902C= NP_937801.1:p.Ser301=
NM_198159.3:c.1223C= NP_937802.1:p.Ser408=
NM_198177.3:c.1175C= NP_937820.1:p.Ser392=
NM_198178.3:c.734C= NP_937821.2:p.Ser245=
NM_000248.4:c.920C= MANE Plus Clinical NP_000239.1:p.Ser307=
NM_006722.3:c.1220C= NP_006713.1:p.Ser407=