Canonical Allele Identifier: CA1373414452
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965164C= , CM000665.2:g.69965164C= GRCh38
NC_000003.11:g.70014315C= , CM000665.1:g.70014315C= GRCh37
NC_000003.10:g.70097005C= NCBI36
NG_011631.1:g.230683C= , LRG_776:g.230683C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1431C= ENSP00000324443.5:p.Leu477=
ENST00000687384.1:c.1428C= ENSP00000510225.1:p.Leu476=
ENST00000689390.1:n.1653C=
ENST00000693031.1:c.1404C= ENSP00000509845.1:p.Leu468=
ENST00000693549.1:c.*242C= ENSP00000509358.1:n.*242C=
ENST00000314589.10:c.1431C= ENSP00000324443.5:p.Leu477=
ENST00000352241.9:c.1497C= MANE Select ENSP00000295600.8:p.Leu499=
ENST00000394351.9:c.1176C= MANE Plus Clinical ENSP00000377880.3:p.Leu392=
ENST00000448226.9:c.1476C= ENSP00000391803.3:p.Leu492=
ENST00000642352.1:c.1479C= ENSP00000494105.1:p.Leu493=
ENST00000314557.10:c.1158C= ENSP00000324246.6:p.Leu386=
ENST00000314589.9:c.1431C= ENSP00000324443.5:p.Leu477=
ENST00000328528.10:c.1476C= ENSP00000327867.6:p.Leu492=
ENST00000352241.8:c.1479C= ENSP00000295600.7:p.Leu493=
ENST00000394351.7:c.1176C= ENSP00000377880.3:p.Leu392=
ENST00000448226.6:c.1497C= ENSP00000391803.2:p.Leu499=
ENST00000472437.5:c.1323C= ENSP00000418845.1:p.Leu441=
ENST00000478490.5:c.*823C= ENSP00000433487.1:n.*823C=
ENST00000531774.1:c.990C= ENSP00000435909.1:p.Leu330=
NM_000248.3:c.1176C= , LRG_776t1:c.1176C= NP_000239.1:p.Leu392=
NM_001184967.1:c.1323C= NP_001171896.1:p.Leu441=
NM_006722.2:c.1476C= NP_006713.1:p.Leu492=
NM_198158.2:c.1158C= NP_937801.1:p.Leu386=
NM_198159.2:c.1479C= NP_937802.1:p.Leu493=
NM_198177.2:c.1431C= NP_937820.1:p.Leu477=
NM_198178.2:c.990C= NP_937821.2:p.Leu330=
XM_005264754.1:c.1497C= XP_005264811.1:p.Leu499=
XM_005264755.2:c.1449C= XP_005264812.1:p.Leu483=
XM_006713164.2:c.1341C= XP_006713227.1:p.Leu447=
XM_011533722.1:c.1494C= XP_011532024.1:p.Leu498=
XM_011533723.1:c.1446C= XP_011532025.1:p.Leu482=
XM_011533724.1:c.1341C= XP_011532026.1:p.Leu447=
XM_011533725.1:c.1329C= XP_011532027.1:p.Leu443=
XM_011533726.1:c.1311C= XP_011532028.1:p.Leu437=
NM_001354604.1:c.1497C= NP_001341533.1:p.Leu499=
NM_001354605.1:c.1494C= NP_001341534.1:p.Leu498=
NM_001354606.1:c.1476C= NP_001341535.1:p.Leu492=
NM_001354607.1:c.1428C= NP_001341536.1:p.Leu476=
NM_001354608.1:c.1323C= NP_001341537.1:p.Leu441=
NM_001184967.2:c.1323C= NP_001171896.1:p.Leu441=
NM_001354604.2:c.1497C= MANE Select NP_001341533.1:p.Leu499=
NM_001354605.2:c.1494C= NP_001341534.1:p.Leu498=
NM_001354606.2:c.1476C= NP_001341535.1:p.Leu492=
NM_001354607.2:c.1428C= NP_001341536.1:p.Leu476=
NM_001354608.2:c.1323C= NP_001341537.1:p.Leu441=
NM_198158.3:c.1158C= NP_937801.1:p.Leu386=
NM_198159.3:c.1479C= NP_937802.1:p.Leu493=
NM_198177.3:c.1431C= NP_937820.1:p.Leu477=
NM_198178.3:c.990C= NP_937821.2:p.Leu330=
NM_000248.4:c.1176C= MANE Plus Clinical NP_000239.1:p.Leu392=
NM_006722.3:c.1476C= NP_006713.1:p.Leu492=