Canonical Allele Identifier: CA1373414435
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965154C= , CM000665.2:g.69965154C= GRCh38
NC_000003.11:g.70014305C= , CM000665.1:g.70014305C= GRCh37
NC_000003.10:g.70096995C= NCBI36
NG_011631.1:g.230673C= , LRG_776:g.230673C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1421C= ENSP00000324443.5:p.Thr474=
ENST00000687384.1:c.1418C= ENSP00000510225.1:p.Thr473=
ENST00000689390.1:n.1643C=
ENST00000693031.1:c.1394C= ENSP00000509845.1:p.Thr465=
ENST00000693549.1:c.*232C= ENSP00000509358.1:n.*232C=
ENST00000314589.10:c.1421C= ENSP00000324443.5:p.Thr474=
ENST00000352241.9:c.1487C= MANE Select ENSP00000295600.8:p.Thr496=
ENST00000394351.9:c.1166C= MANE Plus Clinical ENSP00000377880.3:p.Thr389=
ENST00000448226.9:c.1466C= ENSP00000391803.3:p.Thr489=
ENST00000642352.1:c.1469C= ENSP00000494105.1:p.Thr490=
ENST00000314557.10:c.1148C= ENSP00000324246.6:p.Thr383=
ENST00000314589.9:c.1421C= ENSP00000324443.5:p.Thr474=
ENST00000328528.10:c.1466C= ENSP00000327867.6:p.Thr489=
ENST00000352241.8:c.1469C= ENSP00000295600.7:p.Thr490=
ENST00000394351.7:c.1166C= ENSP00000377880.3:p.Thr389=
ENST00000448226.6:c.1487C= ENSP00000391803.2:p.Thr496=
ENST00000472437.5:c.1313C= ENSP00000418845.1:p.Thr438=
ENST00000478490.5:c.*813C= ENSP00000433487.1:n.*813C=
ENST00000531774.1:c.980C= ENSP00000435909.1:p.Thr327=
NM_000248.3:c.1166C= , LRG_776t1:c.1166C= NP_000239.1:p.Thr389=
NM_001184967.1:c.1313C= NP_001171896.1:p.Thr438=
NM_006722.2:c.1466C= NP_006713.1:p.Thr489=
NM_198158.2:c.1148C= NP_937801.1:p.Thr383=
NM_198159.2:c.1469C= NP_937802.1:p.Thr490=
NM_198177.2:c.1421C= NP_937820.1:p.Thr474=
NM_198178.2:c.980C= NP_937821.2:p.Thr327=
XM_005264754.1:c.1487C= XP_005264811.1:p.Thr496=
XM_005264755.2:c.1439C= XP_005264812.1:p.Thr480=
XM_006713164.2:c.1331C= XP_006713227.1:p.Thr444=
XM_011533722.1:c.1484C= XP_011532024.1:p.Thr495=
XM_011533723.1:c.1436C= XP_011532025.1:p.Thr479=
XM_011533724.1:c.1331C= XP_011532026.1:p.Thr444=
XM_011533725.1:c.1319C= XP_011532027.1:p.Thr440=
XM_011533726.1:c.1301C= XP_011532028.1:p.Thr434=
NM_001354604.1:c.1487C= NP_001341533.1:p.Thr496=
NM_001354605.1:c.1484C= NP_001341534.1:p.Thr495=
NM_001354606.1:c.1466C= NP_001341535.1:p.Thr489=
NM_001354607.1:c.1418C= NP_001341536.1:p.Thr473=
NM_001354608.1:c.1313C= NP_001341537.1:p.Thr438=
NM_001184967.2:c.1313C= NP_001171896.1:p.Thr438=
NM_001354604.2:c.1487C= MANE Select NP_001341533.1:p.Thr496=
NM_001354605.2:c.1484C= NP_001341534.1:p.Thr495=
NM_001354606.2:c.1466C= NP_001341535.1:p.Thr489=
NM_001354607.2:c.1418C= NP_001341536.1:p.Thr473=
NM_001354608.2:c.1313C= NP_001341537.1:p.Thr438=
NM_198158.3:c.1148C= NP_937801.1:p.Thr383=
NM_198159.3:c.1469C= NP_937802.1:p.Thr490=
NM_198177.3:c.1421C= NP_937820.1:p.Thr474=
NM_198178.3:c.980C= NP_937821.2:p.Thr327=
NM_000248.4:c.1166C= MANE Plus Clinical NP_000239.1:p.Thr389=
NM_006722.3:c.1466C= NP_006713.1:p.Thr489=