Canonical Allele Identifier: CA1373447915
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69956525T= , CM000665.2:g.69956525T= GRCh38
NC_000003.11:g.70005676T= , CM000665.1:g.70005676T= GRCh37
NC_000003.10:g.70088366T= NCBI36
NG_011631.1:g.222044T= , LRG_776:g.222044T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.960T= ENSP00000324443.5:p.Asn320=
ENST00000687384.1:c.957T= ENSP00000510225.1:p.Asn319=
ENST00000689390.1:n.1182T=
ENST00000693031.1:c.933T= ENSP00000509845.1:p.Asn311=
ENST00000693549.1:c.960T= ENSP00000509358.1:p.Asn320=
ENST00000314589.10:c.960T= ENSP00000324443.5:p.Asn320=
ENST00000352241.9:c.1026T= MANE Select ENSP00000295600.8:p.Asn342=
ENST00000394351.9:c.705T= MANE Plus Clinical ENSP00000377880.3:p.Asn235=
ENST00000448226.9:c.1005T= ENSP00000391803.3:p.Asn335=
ENST00000642352.1:c.1008T= ENSP00000494105.1:p.Asn336=
ENST00000314557.10:c.687T= ENSP00000324246.6:p.Asn229=
ENST00000314589.9:c.960T= ENSP00000324443.5:p.Asn320=
ENST00000328528.10:c.1005T= ENSP00000327867.6:p.Asn335=
ENST00000352241.8:c.1008T= ENSP00000295600.7:p.Asn336=
ENST00000394351.7:c.705T= ENSP00000377880.3:p.Asn235=
ENST00000448226.6:c.1026T= ENSP00000391803.2:p.Asn342=
ENST00000451708.5:c.978T= ENSP00000398639.1:p.Asn326=
ENST00000472437.5:c.852T= ENSP00000418845.1:p.Asn284=
ENST00000478490.5:c.*352T= ENSP00000433487.1:n.*352T=
ENST00000531774.1:c.519T= ENSP00000435909.1:p.Asn173=
NM_000248.3:c.705T= , LRG_776t1:c.705T= NP_000239.1:p.Asn235=
NM_001184967.1:c.852T= NP_001171896.1:p.Asn284=
NM_006722.2:c.1005T= NP_006713.1:p.Asn335=
NM_198158.2:c.687T= NP_937801.1:p.Asn229=
NM_198159.2:c.1008T= NP_937802.1:p.Asn336=
NM_198177.2:c.960T= NP_937820.1:p.Asn320=
NM_198178.2:c.519T= NP_937821.2:p.Asn173=
XM_005264754.1:c.1026T= XP_005264811.1:p.Asn342=
XM_005264755.2:c.978T= XP_005264812.1:p.Asn326=
XM_006713164.2:c.870T= XP_006713227.1:p.Asn290=
XM_011533722.1:c.1023T= XP_011532024.1:p.Asn341=
XM_011533723.1:c.975T= XP_011532025.1:p.Asn325=
XM_011533724.1:c.870T= XP_011532026.1:p.Asn290=
XM_011533725.1:c.858T= XP_011532027.1:p.Asn286=
XM_011533726.1:c.840T= XP_011532028.1:p.Asn280=
NM_001354604.1:c.1026T= NP_001341533.1:p.Asn342=
NM_001354605.1:c.1023T= NP_001341534.1:p.Asn341=
NM_001354606.1:c.1005T= NP_001341535.1:p.Asn335=
NM_001354607.1:c.957T= NP_001341536.1:p.Asn319=
NM_001354608.1:c.852T= NP_001341537.1:p.Asn284=
NM_001184967.2:c.852T= NP_001171896.1:p.Asn284=
NM_001354604.2:c.1026T= MANE Select NP_001341533.1:p.Asn342=
NM_001354605.2:c.1023T= NP_001341534.1:p.Asn341=
NM_001354606.2:c.1005T= NP_001341535.1:p.Asn335=
NM_001354607.2:c.957T= NP_001341536.1:p.Asn319=
NM_001354608.2:c.852T= NP_001341537.1:p.Asn284=
NM_198158.3:c.687T= NP_937801.1:p.Asn229=
NM_198159.3:c.1008T= NP_937802.1:p.Asn336=
NM_198177.3:c.960T= NP_937820.1:p.Asn320=
NM_198178.3:c.519T= NP_937821.2:p.Asn173=
NM_000248.4:c.705T= MANE Plus Clinical NP_000239.1:p.Asn235=
NM_006722.3:c.1005T= NP_006713.1:p.Asn335=