Canonical Allele Identifier: CA1373443547
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69951856G= , CM000665.2:g.69951856G= GRCh38
NC_000003.11:g.70001007G= , CM000665.1:g.70001007G= GRCh37
NC_000003.10:g.70083697G= NCBI36
NG_011631.1:g.217375G= , LRG_776:g.217375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.859G= ENSP00000324443.5:p.Glu287=
ENST00000687384.1:c.856G= ENSP00000510225.1:p.Glu286=
ENST00000689390.1:n.1081G=
ENST00000693031.1:c.832G= ENSP00000509845.1:p.Glu278=
ENST00000693549.1:c.859G= ENSP00000509358.1:p.Glu287=
ENST00000314589.10:c.859G= ENSP00000324443.5:p.Glu287=
ENST00000352241.9:c.925G= MANE Select ENSP00000295600.8:p.Glu309=
ENST00000394351.9:c.604G= MANE Plus Clinical ENSP00000377880.3:p.Glu202=
ENST00000448226.9:c.904G= ENSP00000391803.3:p.Glu302=
ENST00000642352.1:c.907G= ENSP00000494105.1:p.Glu303=
ENST00000314557.10:c.586G= ENSP00000324246.6:p.Glu196=
ENST00000314589.9:c.859G= ENSP00000324443.5:p.Glu287=
ENST00000328528.10:c.904G= ENSP00000327867.6:p.Glu302=
ENST00000352241.8:c.907G= ENSP00000295600.7:p.Glu303=
ENST00000394351.7:c.604G= ENSP00000377880.3:p.Glu202=
ENST00000448226.6:c.925G= ENSP00000391803.2:p.Glu309=
ENST00000451708.5:c.877G= ENSP00000398639.1:p.Glu293=
ENST00000472437.5:c.751G= ENSP00000418845.1:p.Glu251=
ENST00000478490.5:c.*251G= ENSP00000433487.1:n.*251G=
ENST00000531774.1:c.418G= ENSP00000435909.1:p.Glu140=
NM_000248.3:c.604G= , LRG_776t1:c.604G= NP_000239.1:p.Glu202=
NM_001184967.1:c.751G= NP_001171896.1:p.Glu251=
NM_006722.2:c.904G= NP_006713.1:p.Glu302=
NM_198158.2:c.586G= NP_937801.1:p.Glu196=
NM_198159.2:c.907G= NP_937802.1:p.Glu303=
NM_198177.2:c.859G= NP_937820.1:p.Glu287=
NM_198178.2:c.418G= NP_937821.2:p.Glu140=
XM_005264754.1:c.925G= XP_005264811.1:p.Glu309=
XM_005264755.2:c.877G= XP_005264812.1:p.Glu293=
XM_006713164.2:c.769G= XP_006713227.1:p.Glu257=
XM_011533722.1:c.922G= XP_011532024.1:p.Glu308=
XM_011533723.1:c.874G= XP_011532025.1:p.Glu292=
XM_011533724.1:c.769G= XP_011532026.1:p.Glu257=
XM_011533725.1:c.757G= XP_011532027.1:p.Glu253=
XM_011533726.1:c.739G= XP_011532028.1:p.Glu247=
NM_001354604.1:c.925G= NP_001341533.1:p.Glu309=
NM_001354605.1:c.922G= NP_001341534.1:p.Glu308=
NM_001354606.1:c.904G= NP_001341535.1:p.Glu302=
NM_001354607.1:c.856G= NP_001341536.1:p.Glu286=
NM_001354608.1:c.751G= NP_001341537.1:p.Glu251=
NM_001184967.2:c.751G= NP_001171896.1:p.Glu251=
NM_001354604.2:c.925G= MANE Select NP_001341533.1:p.Glu309=
NM_001354605.2:c.922G= NP_001341534.1:p.Glu308=
NM_001354606.2:c.904G= NP_001341535.1:p.Glu302=
NM_001354607.2:c.856G= NP_001341536.1:p.Glu286=
NM_001354608.2:c.751G= NP_001341537.1:p.Glu251=
NM_198158.3:c.586G= NP_937801.1:p.Glu196=
NM_198159.3:c.907G= NP_937802.1:p.Glu303=
NM_198177.3:c.859G= NP_937820.1:p.Glu287=
NM_198178.3:c.418G= NP_937821.2:p.Glu140=
NM_000248.4:c.604G= MANE Plus Clinical NP_000239.1:p.Glu202=
NM_006722.3:c.904G= NP_006713.1:p.Glu302=