Canonical Allele Identifier: CA1373414471
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965180C= , CM000665.2:g.69965180C= GRCh38
NC_000003.11:g.70014331C= , CM000665.1:g.70014331C= GRCh37
NC_000003.10:g.70097021C= NCBI36
NG_011631.1:g.230699C= , LRG_776:g.230699C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1447C= ENSP00000324443.5:p.Pro483=
ENST00000687384.1:c.1444C= ENSP00000510225.1:p.Pro482=
ENST00000689390.1:n.1669C=
ENST00000693031.1:c.1420C= ENSP00000509845.1:p.Pro474=
ENST00000693549.1:c.*258C= ENSP00000509358.1:n.*258C=
ENST00000314589.10:c.1447C= ENSP00000324443.5:p.Pro483=
ENST00000352241.9:c.1513C= MANE Select ENSP00000295600.8:p.Pro505=
ENST00000394351.9:c.1192C= MANE Plus Clinical ENSP00000377880.3:p.Pro398=
ENST00000448226.9:c.1492C= ENSP00000391803.3:p.Pro498=
ENST00000642352.1:c.1495C= ENSP00000494105.1:p.Pro499=
ENST00000314557.10:c.1174C= ENSP00000324246.6:p.Pro392=
ENST00000314589.9:c.1447C= ENSP00000324443.5:p.Pro483=
ENST00000328528.10:c.1492C= ENSP00000327867.6:p.Pro498=
ENST00000352241.8:c.1495C= ENSP00000295600.7:p.Pro499=
ENST00000394351.7:c.1192C= ENSP00000377880.3:p.Pro398=
ENST00000448226.6:c.1513C= ENSP00000391803.2:p.Pro505=
ENST00000472437.5:c.1339C= ENSP00000418845.1:p.Pro447=
ENST00000478490.5:c.*839C= ENSP00000433487.1:n.*839C=
ENST00000531774.1:c.1006C= ENSP00000435909.1:p.Pro336=
NM_000248.3:c.1192C= , LRG_776t1:c.1192C= NP_000239.1:p.Pro398=
NM_001184967.1:c.1339C= NP_001171896.1:p.Pro447=
NM_006722.2:c.1492C= NP_006713.1:p.Pro498=
NM_198158.2:c.1174C= NP_937801.1:p.Pro392=
NM_198159.2:c.1495C= NP_937802.1:p.Pro499=
NM_198177.2:c.1447C= NP_937820.1:p.Pro483=
NM_198178.2:c.1006C= NP_937821.2:p.Pro336=
XM_005264754.1:c.1513C= XP_005264811.1:p.Pro505=
XM_005264755.2:c.1465C= XP_005264812.1:p.Pro489=
XM_006713164.2:c.1357C= XP_006713227.1:p.Pro453=
XM_011533722.1:c.1510C= XP_011532024.1:p.Pro504=
XM_011533723.1:c.1462C= XP_011532025.1:p.Pro488=
XM_011533724.1:c.1357C= XP_011532026.1:p.Pro453=
XM_011533725.1:c.1345C= XP_011532027.1:p.Pro449=
XM_011533726.1:c.1327C= XP_011532028.1:p.Pro443=
NM_001354604.1:c.1513C= NP_001341533.1:p.Pro505=
NM_001354605.1:c.1510C= NP_001341534.1:p.Pro504=
NM_001354606.1:c.1492C= NP_001341535.1:p.Pro498=
NM_001354607.1:c.1444C= NP_001341536.1:p.Pro482=
NM_001354608.1:c.1339C= NP_001341537.1:p.Pro447=
NM_001184967.2:c.1339C= NP_001171896.1:p.Pro447=
NM_001354604.2:c.1513C= MANE Select NP_001341533.1:p.Pro505=
NM_001354605.2:c.1510C= NP_001341534.1:p.Pro504=
NM_001354606.2:c.1492C= NP_001341535.1:p.Pro498=
NM_001354607.2:c.1444C= NP_001341536.1:p.Pro482=
NM_001354608.2:c.1339C= NP_001341537.1:p.Pro447=
NM_198158.3:c.1174C= NP_937801.1:p.Pro392=
NM_198159.3:c.1495C= NP_937802.1:p.Pro499=
NM_198177.3:c.1447C= NP_937820.1:p.Pro483=
NM_198178.3:c.1006C= NP_937821.2:p.Pro336=
NM_000248.4:c.1192C= MANE Plus Clinical NP_000239.1:p.Pro398=
NM_006722.3:c.1492C= NP_006713.1:p.Pro498=