Canonical Allele Identifier: CA1373414461
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965173A= , CM000665.2:g.69965173A= GRCh38
NC_000003.11:g.70014324A= , CM000665.1:g.70014324A= GRCh37
NC_000003.10:g.70097014A= NCBI36
NG_011631.1:g.230692A= , LRG_776:g.230692A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1440A= ENSP00000324443.5:p.Ser480=
ENST00000687384.1:c.1437A= ENSP00000510225.1:p.Ser479=
ENST00000689390.1:n.1662A=
ENST00000693031.1:c.1413A= ENSP00000509845.1:p.Ser471=
ENST00000693549.1:c.*251A= ENSP00000509358.1:n.*251A=
ENST00000314589.10:c.1440A= ENSP00000324443.5:p.Ser480=
ENST00000352241.9:c.1506A= MANE Select ENSP00000295600.8:p.Ser502=
ENST00000394351.9:c.1185A= MANE Plus Clinical ENSP00000377880.3:p.Ser395=
ENST00000448226.9:c.1485A= ENSP00000391803.3:p.Ser495=
ENST00000642352.1:c.1488A= ENSP00000494105.1:p.Ser496=
ENST00000314557.10:c.1167A= ENSP00000324246.6:p.Ser389=
ENST00000314589.9:c.1440A= ENSP00000324443.5:p.Ser480=
ENST00000328528.10:c.1485A= ENSP00000327867.6:p.Ser495=
ENST00000352241.8:c.1488A= ENSP00000295600.7:p.Ser496=
ENST00000394351.7:c.1185A= ENSP00000377880.3:p.Ser395=
ENST00000448226.6:c.1506A= ENSP00000391803.2:p.Ser502=
ENST00000472437.5:c.1332A= ENSP00000418845.1:p.Ser444=
ENST00000478490.5:c.*832A= ENSP00000433487.1:n.*832A=
ENST00000531774.1:c.999A= ENSP00000435909.1:p.Ser333=
NM_000248.3:c.1185A= , LRG_776t1:c.1185A= NP_000239.1:p.Ser395=
NM_001184967.1:c.1332A= NP_001171896.1:p.Ser444=
NM_006722.2:c.1485A= NP_006713.1:p.Ser495=
NM_198158.2:c.1167A= NP_937801.1:p.Ser389=
NM_198159.2:c.1488A= NP_937802.1:p.Ser496=
NM_198177.2:c.1440A= NP_937820.1:p.Ser480=
NM_198178.2:c.999A= NP_937821.2:p.Ser333=
XM_005264754.1:c.1506A= XP_005264811.1:p.Ser502=
XM_005264755.2:c.1458A= XP_005264812.1:p.Ser486=
XM_006713164.2:c.1350A= XP_006713227.1:p.Ser450=
XM_011533722.1:c.1503A= XP_011532024.1:p.Ser501=
XM_011533723.1:c.1455A= XP_011532025.1:p.Ser485=
XM_011533724.1:c.1350A= XP_011532026.1:p.Ser450=
XM_011533725.1:c.1338A= XP_011532027.1:p.Ser446=
XM_011533726.1:c.1320A= XP_011532028.1:p.Ser440=
NM_001354604.1:c.1506A= NP_001341533.1:p.Ser502=
NM_001354605.1:c.1503A= NP_001341534.1:p.Ser501=
NM_001354606.1:c.1485A= NP_001341535.1:p.Ser495=
NM_001354607.1:c.1437A= NP_001341536.1:p.Ser479=
NM_001354608.1:c.1332A= NP_001341537.1:p.Ser444=
NM_001184967.2:c.1332A= NP_001171896.1:p.Ser444=
NM_001354604.2:c.1506A= MANE Select NP_001341533.1:p.Ser502=
NM_001354605.2:c.1503A= NP_001341534.1:p.Ser501=
NM_001354606.2:c.1485A= NP_001341535.1:p.Ser495=
NM_001354607.2:c.1437A= NP_001341536.1:p.Ser479=
NM_001354608.2:c.1332A= NP_001341537.1:p.Ser444=
NM_198158.3:c.1167A= NP_937801.1:p.Ser389=
NM_198159.3:c.1488A= NP_937802.1:p.Ser496=
NM_198177.3:c.1440A= NP_937820.1:p.Ser480=
NM_198178.3:c.999A= NP_937821.2:p.Ser333=
NM_000248.4:c.1185A= MANE Plus Clinical NP_000239.1:p.Ser395=
NM_006722.3:c.1485A= NP_006713.1:p.Ser495=