Canonical Allele Identifier: CA1373413942
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69964900T= , CM000665.2:g.69964900T= GRCh38
NC_000003.11:g.70014051T= , CM000665.1:g.70014051T= GRCh37
NC_000003.10:g.70096741T= NCBI36
NG_011631.1:g.230419T= , LRG_776:g.230419T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1167T= ENSP00000324443.5:p.Gly389=
ENST00000687384.1:c.1164T= ENSP00000510225.1:p.Gly388=
ENST00000689390.1:n.1389T=
ENST00000693031.1:c.1140T= ENSP00000509845.1:p.Gly380=
ENST00000693549.1:c.1114-14T= ENSP00000509358.1:n.1114-14T=
ENST00000314589.10:c.1167T= ENSP00000324443.5:p.Gly389=
ENST00000352241.9:c.1233T= MANE Select ENSP00000295600.8:p.Gly411=
ENST00000394351.9:c.912T= MANE Plus Clinical ENSP00000377880.3:p.Gly304=
ENST00000448226.9:c.1212T= ENSP00000391803.3:p.Gly404=
ENST00000642352.1:c.1215T= ENSP00000494105.1:p.Gly405=
ENST00000314557.10:c.894T= ENSP00000324246.6:p.Gly298=
ENST00000314589.9:c.1167T= ENSP00000324443.5:p.Gly389=
ENST00000328528.10:c.1212T= ENSP00000327867.6:p.Gly404=
ENST00000352241.8:c.1215T= ENSP00000295600.7:p.Gly405=
ENST00000394351.7:c.912T= ENSP00000377880.3:p.Gly304=
ENST00000448226.6:c.1233T= ENSP00000391803.2:p.Gly411=
ENST00000472437.5:c.1059T= ENSP00000418845.1:p.Gly353=
ENST00000478490.5:c.*559T= ENSP00000433487.1:n.*559T=
ENST00000531774.1:c.726T= ENSP00000435909.1:p.Gly242=
NM_000248.3:c.912T= , LRG_776t1:c.912T= NP_000239.1:p.Gly304=
NM_001184967.1:c.1059T= NP_001171896.1:p.Gly353=
NM_006722.2:c.1212T= NP_006713.1:p.Gly404=
NM_198158.2:c.894T= NP_937801.1:p.Gly298=
NM_198159.2:c.1215T= NP_937802.1:p.Gly405=
NM_198177.2:c.1167T= NP_937820.1:p.Gly389=
NM_198178.2:c.726T= NP_937821.2:p.Gly242=
XM_005264754.1:c.1233T= XP_005264811.1:p.Gly411=
XM_005264755.2:c.1185T= XP_005264812.1:p.Gly395=
XM_006713164.2:c.1077T= XP_006713227.1:p.Gly359=
XM_011533722.1:c.1230T= XP_011532024.1:p.Gly410=
XM_011533723.1:c.1182T= XP_011532025.1:p.Gly394=
XM_011533724.1:c.1077T= XP_011532026.1:p.Gly359=
XM_011533725.1:c.1065T= XP_011532027.1:p.Gly355=
XM_011533726.1:c.1047T= XP_011532028.1:p.Gly349=
NM_001354604.1:c.1233T= NP_001341533.1:p.Gly411=
NM_001354605.1:c.1230T= NP_001341534.1:p.Gly410=
NM_001354606.1:c.1212T= NP_001341535.1:p.Gly404=
NM_001354607.1:c.1164T= NP_001341536.1:p.Gly388=
NM_001354608.1:c.1059T= NP_001341537.1:p.Gly353=
NM_001184967.2:c.1059T= NP_001171896.1:p.Gly353=
NM_001354604.2:c.1233T= MANE Select NP_001341533.1:p.Gly411=
NM_001354605.2:c.1230T= NP_001341534.1:p.Gly410=
NM_001354606.2:c.1212T= NP_001341535.1:p.Gly404=
NM_001354607.2:c.1164T= NP_001341536.1:p.Gly388=
NM_001354608.2:c.1059T= NP_001341537.1:p.Gly353=
NM_198158.3:c.894T= NP_937801.1:p.Gly298=
NM_198159.3:c.1215T= NP_937802.1:p.Gly405=
NM_198177.3:c.1167T= NP_937820.1:p.Gly389=
NM_198178.3:c.726T= NP_937821.2:p.Gly242=
NM_000248.4:c.912T= MANE Plus Clinical NP_000239.1:p.Gly304=
NM_006722.3:c.1212T= NP_006713.1:p.Gly404=