Canonical Allele Identifier: CA1373413930
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69964896C= , CM000665.2:g.69964896C= GRCh38
NC_000003.11:g.70014047C= , CM000665.1:g.70014047C= GRCh37
NC_000003.10:g.70096737C= NCBI36
NG_011631.1:g.230415C= , LRG_776:g.230415C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1163C= ENSP00000324443.5:p.Thr388=
ENST00000687384.1:c.1160C= ENSP00000510225.1:p.Thr387=
ENST00000689390.1:n.1385C=
ENST00000693031.1:c.1136C= ENSP00000509845.1:p.Thr379=
ENST00000693549.1:c.1114-18C= ENSP00000509358.1:n.1114-18C=
ENST00000314589.10:c.1163C= ENSP00000324443.5:p.Thr388=
ENST00000352241.9:c.1229C= MANE Select ENSP00000295600.8:p.Thr410=
ENST00000394351.9:c.908C= MANE Plus Clinical ENSP00000377880.3:p.Thr303=
ENST00000448226.9:c.1208C= ENSP00000391803.3:p.Thr403=
ENST00000642352.1:c.1211C= ENSP00000494105.1:p.Thr404=
ENST00000314557.10:c.890C= ENSP00000324246.6:p.Thr297=
ENST00000314589.9:c.1163C= ENSP00000324443.5:p.Thr388=
ENST00000328528.10:c.1208C= ENSP00000327867.6:p.Thr403=
ENST00000352241.8:c.1211C= ENSP00000295600.7:p.Thr404=
ENST00000394351.7:c.908C= ENSP00000377880.3:p.Thr303=
ENST00000448226.6:c.1229C= ENSP00000391803.2:p.Thr410=
ENST00000472437.5:c.1055C= ENSP00000418845.1:p.Thr352=
ENST00000478490.5:c.*555C= ENSP00000433487.1:n.*555C=
ENST00000531774.1:c.722C= ENSP00000435909.1:p.Thr241=
NM_000248.3:c.908C= , LRG_776t1:c.908C= NP_000239.1:p.Thr303=
NM_001184967.1:c.1055C= NP_001171896.1:p.Thr352=
NM_006722.2:c.1208C= NP_006713.1:p.Thr403=
NM_198158.2:c.890C= NP_937801.1:p.Thr297=
NM_198159.2:c.1211C= NP_937802.1:p.Thr404=
NM_198177.2:c.1163C= NP_937820.1:p.Thr388=
NM_198178.2:c.722C= NP_937821.2:p.Thr241=
XM_005264754.1:c.1229C= XP_005264811.1:p.Thr410=
XM_005264755.2:c.1181C= XP_005264812.1:p.Thr394=
XM_006713164.2:c.1073C= XP_006713227.1:p.Thr358=
XM_011533722.1:c.1226C= XP_011532024.1:p.Thr409=
XM_011533723.1:c.1178C= XP_011532025.1:p.Thr393=
XM_011533724.1:c.1073C= XP_011532026.1:p.Thr358=
XM_011533725.1:c.1061C= XP_011532027.1:p.Thr354=
XM_011533726.1:c.1043C= XP_011532028.1:p.Thr348=
NM_001354604.1:c.1229C= NP_001341533.1:p.Thr410=
NM_001354605.1:c.1226C= NP_001341534.1:p.Thr409=
NM_001354606.1:c.1208C= NP_001341535.1:p.Thr403=
NM_001354607.1:c.1160C= NP_001341536.1:p.Thr387=
NM_001354608.1:c.1055C= NP_001341537.1:p.Thr352=
NM_001184967.2:c.1055C= NP_001171896.1:p.Thr352=
NM_001354604.2:c.1229C= MANE Select NP_001341533.1:p.Thr410=
NM_001354605.2:c.1226C= NP_001341534.1:p.Thr409=
NM_001354606.2:c.1208C= NP_001341535.1:p.Thr403=
NM_001354607.2:c.1160C= NP_001341536.1:p.Thr387=
NM_001354608.2:c.1055C= NP_001341537.1:p.Thr352=
NM_198158.3:c.890C= NP_937801.1:p.Thr297=
NM_198159.3:c.1211C= NP_937802.1:p.Thr404=
NM_198177.3:c.1163C= NP_937820.1:p.Thr388=
NM_198178.3:c.722C= NP_937821.2:p.Thr241=
NM_000248.4:c.908C= MANE Plus Clinical NP_000239.1:p.Thr303=
NM_006722.3:c.1208C= NP_006713.1:p.Thr403=