Canonical Allele Identifier: CA1373447903
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69956503G= , CM000665.2:g.69956503G= GRCh38
NC_000003.11:g.70005654G= , CM000665.1:g.70005654G= GRCh37
NC_000003.10:g.70088344G= NCBI36
NG_011631.1:g.222022G= , LRG_776:g.222022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.938G= ENSP00000324443.5:p.Gly313=
ENST00000687384.1:c.935G= ENSP00000510225.1:p.Gly312=
ENST00000689390.1:n.1160G=
ENST00000693031.1:c.911G= ENSP00000509845.1:p.Gly304=
ENST00000693549.1:c.938G= ENSP00000509358.1:p.Gly313=
ENST00000314589.10:c.938G= ENSP00000324443.5:p.Gly313=
ENST00000352241.9:c.1004G= MANE Select ENSP00000295600.8:p.Gly335=
ENST00000394351.9:c.683G= MANE Plus Clinical ENSP00000377880.3:p.Gly228=
ENST00000448226.9:c.983G= ENSP00000391803.3:p.Gly328=
ENST00000642352.1:c.986G= ENSP00000494105.1:p.Gly329=
ENST00000314557.10:c.665G= ENSP00000324246.6:p.Gly222=
ENST00000314589.9:c.938G= ENSP00000324443.5:p.Gly313=
ENST00000328528.10:c.983G= ENSP00000327867.6:p.Gly328=
ENST00000352241.8:c.986G= ENSP00000295600.7:p.Gly329=
ENST00000394351.7:c.683G= ENSP00000377880.3:p.Gly228=
ENST00000448226.6:c.1004G= ENSP00000391803.2:p.Gly335=
ENST00000451708.5:c.956G= ENSP00000398639.1:p.Gly319=
ENST00000472437.5:c.830G= ENSP00000418845.1:p.Gly277=
ENST00000478490.5:c.*330G= ENSP00000433487.1:n.*330G=
ENST00000531774.1:c.497G= ENSP00000435909.1:p.Gly166=
NM_000248.3:c.683G= , LRG_776t1:c.683G= NP_000239.1:p.Gly228=
NM_001184967.1:c.830G= NP_001171896.1:p.Gly277=
NM_006722.2:c.983G= NP_006713.1:p.Gly328=
NM_198158.2:c.665G= NP_937801.1:p.Gly222=
NM_198159.2:c.986G= NP_937802.1:p.Gly329=
NM_198177.2:c.938G= NP_937820.1:p.Gly313=
NM_198178.2:c.497G= NP_937821.2:p.Gly166=
XM_005264754.1:c.1004G= XP_005264811.1:p.Gly335=
XM_005264755.2:c.956G= XP_005264812.1:p.Gly319=
XM_006713164.2:c.848G= XP_006713227.1:p.Gly283=
XM_011533722.1:c.1001G= XP_011532024.1:p.Gly334=
XM_011533723.1:c.953G= XP_011532025.1:p.Gly318=
XM_011533724.1:c.848G= XP_011532026.1:p.Gly283=
XM_011533725.1:c.836G= XP_011532027.1:p.Gly279=
XM_011533726.1:c.818G= XP_011532028.1:p.Gly273=
NM_001354604.1:c.1004G= NP_001341533.1:p.Gly335=
NM_001354605.1:c.1001G= NP_001341534.1:p.Gly334=
NM_001354606.1:c.983G= NP_001341535.1:p.Gly328=
NM_001354607.1:c.935G= NP_001341536.1:p.Gly312=
NM_001354608.1:c.830G= NP_001341537.1:p.Gly277=
NM_001184967.2:c.830G= NP_001171896.1:p.Gly277=
NM_001354604.2:c.1004G= MANE Select NP_001341533.1:p.Gly335=
NM_001354605.2:c.1001G= NP_001341534.1:p.Gly334=
NM_001354606.2:c.983G= NP_001341535.1:p.Gly328=
NM_001354607.2:c.935G= NP_001341536.1:p.Gly312=
NM_001354608.2:c.830G= NP_001341537.1:p.Gly277=
NM_198158.3:c.665G= NP_937801.1:p.Gly222=
NM_198159.3:c.986G= NP_937802.1:p.Gly329=
NM_198177.3:c.938G= NP_937820.1:p.Gly313=
NM_198178.3:c.497G= NP_937821.2:p.Gly166=
NM_000248.4:c.683G= MANE Plus Clinical NP_000239.1:p.Gly228=
NM_006722.3:c.983G= NP_006713.1:p.Gly328=