Canonical Allele Identifier: CA1373414439
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965157A= , CM000665.2:g.69965157A= GRCh38
NC_000003.11:g.70014308A= , CM000665.1:g.70014308A= GRCh37
NC_000003.10:g.70096998A= NCBI36
NG_011631.1:g.230676A= , LRG_776:g.230676A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1424A= ENSP00000324443.5:p.Asp475=
ENST00000687384.1:c.1421A= ENSP00000510225.1:p.Asp474=
ENST00000689390.1:n.1646A=
ENST00000693031.1:c.1397A= ENSP00000509845.1:p.Asp466=
ENST00000693549.1:c.*235A= ENSP00000509358.1:n.*235A=
ENST00000314589.10:c.1424A= ENSP00000324443.5:p.Asp475=
ENST00000352241.9:c.1490A= MANE Select ENSP00000295600.8:p.Asp497=
ENST00000394351.9:c.1169A= MANE Plus Clinical ENSP00000377880.3:p.Asp390=
ENST00000448226.9:c.1469A= ENSP00000391803.3:p.Asp490=
ENST00000642352.1:c.1472A= ENSP00000494105.1:p.Asp491=
ENST00000314557.10:c.1151A= ENSP00000324246.6:p.Asp384=
ENST00000314589.9:c.1424A= ENSP00000324443.5:p.Asp475=
ENST00000328528.10:c.1469A= ENSP00000327867.6:p.Asp490=
ENST00000352241.8:c.1472A= ENSP00000295600.7:p.Asp491=
ENST00000394351.7:c.1169A= ENSP00000377880.3:p.Asp390=
ENST00000448226.6:c.1490A= ENSP00000391803.2:p.Asp497=
ENST00000472437.5:c.1316A= ENSP00000418845.1:p.Asp439=
ENST00000478490.5:c.*816A= ENSP00000433487.1:n.*816A=
ENST00000531774.1:c.983A= ENSP00000435909.1:p.Asp328=
NM_000248.3:c.1169A= , LRG_776t1:c.1169A= NP_000239.1:p.Asp390=
NM_001184967.1:c.1316A= NP_001171896.1:p.Asp439=
NM_006722.2:c.1469A= NP_006713.1:p.Asp490=
NM_198158.2:c.1151A= NP_937801.1:p.Asp384=
NM_198159.2:c.1472A= NP_937802.1:p.Asp491=
NM_198177.2:c.1424A= NP_937820.1:p.Asp475=
NM_198178.2:c.983A= NP_937821.2:p.Asp328=
XM_005264754.1:c.1490A= XP_005264811.1:p.Asp497=
XM_005264755.2:c.1442A= XP_005264812.1:p.Asp481=
XM_006713164.2:c.1334A= XP_006713227.1:p.Asp445=
XM_011533722.1:c.1487A= XP_011532024.1:p.Asp496=
XM_011533723.1:c.1439A= XP_011532025.1:p.Asp480=
XM_011533724.1:c.1334A= XP_011532026.1:p.Asp445=
XM_011533725.1:c.1322A= XP_011532027.1:p.Asp441=
XM_011533726.1:c.1304A= XP_011532028.1:p.Asp435=
NM_001354604.1:c.1490A= NP_001341533.1:p.Asp497=
NM_001354605.1:c.1487A= NP_001341534.1:p.Asp496=
NM_001354606.1:c.1469A= NP_001341535.1:p.Asp490=
NM_001354607.1:c.1421A= NP_001341536.1:p.Asp474=
NM_001354608.1:c.1316A= NP_001341537.1:p.Asp439=
NM_001184967.2:c.1316A= NP_001171896.1:p.Asp439=
NM_001354604.2:c.1490A= MANE Select NP_001341533.1:p.Asp497=
NM_001354605.2:c.1487A= NP_001341534.1:p.Asp496=
NM_001354606.2:c.1469A= NP_001341535.1:p.Asp490=
NM_001354607.2:c.1421A= NP_001341536.1:p.Asp474=
NM_001354608.2:c.1316A= NP_001341537.1:p.Asp439=
NM_198158.3:c.1151A= NP_937801.1:p.Asp384=
NM_198159.3:c.1472A= NP_937802.1:p.Asp491=
NM_198177.3:c.1424A= NP_937820.1:p.Asp475=
NM_198178.3:c.983A= NP_937821.2:p.Asp328=
NM_000248.4:c.1169A= MANE Plus Clinical NP_000239.1:p.Asp390=
NM_006722.3:c.1469A= NP_006713.1:p.Asp490=