Canonical Allele Identifier: CA1373414515
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965203C= , CM000665.2:g.69965203C= GRCh38
NC_000003.11:g.70014354C= , CM000665.1:g.70014354C= GRCh37
NC_000003.10:g.70097044C= NCBI36
NG_011631.1:g.230722C= , LRG_776:g.230722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1470C= ENSP00000324443.5:p.Ser490=
ENST00000687384.1:c.1467C= ENSP00000510225.1:p.Ser489=
ENST00000689390.1:n.1692C=
ENST00000693031.1:c.1443C= ENSP00000509845.1:p.Ser481=
ENST00000693549.1:c.*281C= ENSP00000509358.1:n.*281C=
ENST00000314589.10:c.1470C= ENSP00000324443.5:p.Ser490=
ENST00000352241.9:c.1536C= MANE Select ENSP00000295600.8:p.Ser512=
ENST00000394351.9:c.1215C= MANE Plus Clinical ENSP00000377880.3:p.Ser405=
ENST00000448226.9:c.1515C= ENSP00000391803.3:p.Ser505=
ENST00000642352.1:c.1518C= ENSP00000494105.1:p.Ser506=
ENST00000314557.10:c.1197C= ENSP00000324246.6:p.Ser399=
ENST00000314589.9:c.1470C= ENSP00000324443.5:p.Ser490=
ENST00000328528.10:c.1515C= ENSP00000327867.6:p.Ser505=
ENST00000352241.8:c.1518C= ENSP00000295600.7:p.Ser506=
ENST00000394351.7:c.1215C= ENSP00000377880.3:p.Ser405=
ENST00000448226.6:c.1536C= ENSP00000391803.2:p.Ser512=
ENST00000472437.5:c.1362C= ENSP00000418845.1:p.Ser454=
ENST00000478490.5:c.*862C= ENSP00000433487.1:n.*862C=
ENST00000531774.1:c.1029C= ENSP00000435909.1:p.Ser343=
NM_000248.3:c.1215C= , LRG_776t1:c.1215C= NP_000239.1:p.Ser405=
NM_001184967.1:c.1362C= NP_001171896.1:p.Ser454=
NM_006722.2:c.1515C= NP_006713.1:p.Ser505=
NM_198158.2:c.1197C= NP_937801.1:p.Ser399=
NM_198159.2:c.1518C= NP_937802.1:p.Ser506=
NM_198177.2:c.1470C= NP_937820.1:p.Ser490=
NM_198178.2:c.1029C= NP_937821.2:p.Ser343=
XM_005264754.1:c.1536C= XP_005264811.1:p.Ser512=
XM_005264755.2:c.1488C= XP_005264812.1:p.Ser496=
XM_006713164.2:c.1380C= XP_006713227.1:p.Ser460=
XM_011533722.1:c.1533C= XP_011532024.1:p.Ser511=
XM_011533723.1:c.1485C= XP_011532025.1:p.Ser495=
XM_011533724.1:c.1380C= XP_011532026.1:p.Ser460=
XM_011533725.1:c.1368C= XP_011532027.1:p.Ser456=
XM_011533726.1:c.1350C= XP_011532028.1:p.Ser450=
NM_001354604.1:c.1536C= NP_001341533.1:p.Ser512=
NM_001354605.1:c.1533C= NP_001341534.1:p.Ser511=
NM_001354606.1:c.1515C= NP_001341535.1:p.Ser505=
NM_001354607.1:c.1467C= NP_001341536.1:p.Ser489=
NM_001354608.1:c.1362C= NP_001341537.1:p.Ser454=
NM_001184967.2:c.1362C= NP_001171896.1:p.Ser454=
NM_001354604.2:c.1536C= MANE Select NP_001341533.1:p.Ser512=
NM_001354605.2:c.1533C= NP_001341534.1:p.Ser511=
NM_001354606.2:c.1515C= NP_001341535.1:p.Ser505=
NM_001354607.2:c.1467C= NP_001341536.1:p.Ser489=
NM_001354608.2:c.1362C= NP_001341537.1:p.Ser454=
NM_198158.3:c.1197C= NP_937801.1:p.Ser399=
NM_198159.3:c.1518C= NP_937802.1:p.Ser506=
NM_198177.3:c.1470C= NP_937820.1:p.Ser490=
NM_198178.3:c.1029C= NP_937821.2:p.Ser343=
NM_000248.4:c.1215C= MANE Plus Clinical NP_000239.1:p.Ser405=
NM_006722.3:c.1515C= NP_006713.1:p.Ser505=