Canonical Allele Identifier: CA1373440711
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69949111C= , CM000665.2:g.69949111C= GRCh38
NC_000003.11:g.69998262C= , CM000665.1:g.69998262C= GRCh37
NC_000003.10:g.70080952C= NCBI36
NG_011631.1:g.214630C= , LRG_776:g.214630C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.775C= ENSP00000324443.5:p.Leu259=
ENST00000687384.1:c.772C= ENSP00000510225.1:p.Leu258=
ENST00000689390.1:n.997C=
ENST00000693031.1:c.748C= ENSP00000509845.1:p.Leu250=
ENST00000693549.1:c.775C= ENSP00000509358.1:p.Leu259=
ENST00000314589.10:c.775C= ENSP00000324443.5:p.Leu259=
ENST00000352241.9:c.823C= MANE Select ENSP00000295600.8:p.Leu275=
ENST00000394351.9:c.502C= MANE Plus Clinical ENSP00000377880.3:p.Leu168=
ENST00000448226.9:c.820C= ENSP00000391803.3:p.Leu274=
ENST00000642352.1:c.823C= ENSP00000494105.1:p.Leu275=
ENST00000314557.10:c.502C= ENSP00000324246.6:p.Leu168=
ENST00000314589.9:c.775C= ENSP00000324443.5:p.Leu259=
ENST00000328528.10:c.820C= ENSP00000327867.6:p.Leu274=
ENST00000352241.8:c.823C= ENSP00000295600.7:p.Leu275=
ENST00000394351.7:c.502C= ENSP00000377880.3:p.Leu168=
ENST00000448226.6:c.823C= ENSP00000391803.2:p.Leu275=
ENST00000451708.5:c.775C= ENSP00000398639.1:p.Leu259=
ENST00000472437.5:c.667C= ENSP00000418845.1:p.Leu223=
ENST00000478490.5:c.*149C= ENSP00000433487.1:n.*149C=
ENST00000531774.1:c.334C= ENSP00000435909.1:p.Leu112=
NM_000248.3:c.502C= , LRG_776t1:c.502C= NP_000239.1:p.Leu168=
NM_001184967.1:c.667C= NP_001171896.1:p.Leu223=
NM_006722.2:c.820C= NP_006713.1:p.Leu274=
NM_198158.2:c.502C= NP_937801.1:p.Leu168=
NM_198159.2:c.823C= NP_937802.1:p.Leu275=
NM_198177.2:c.775C= NP_937820.1:p.Leu259=
NM_198178.2:c.334C= NP_937821.2:p.Leu112=
XM_005264754.1:c.823C= XP_005264811.1:p.Leu275=
XM_005264755.2:c.775C= XP_005264812.1:p.Leu259=
XM_006713164.2:c.667C= XP_006713227.1:p.Leu223=
XM_011533722.1:c.820C= XP_011532024.1:p.Leu274=
XM_011533723.1:c.772C= XP_011532025.1:p.Leu258=
XM_011533724.1:c.667C= XP_011532026.1:p.Leu223=
XM_011533725.1:c.655C= XP_011532027.1:p.Leu219=
XM_011533726.1:c.655C= XP_011532028.1:p.Leu219=
NM_001354604.1:c.823C= NP_001341533.1:p.Leu275=
NM_001354605.1:c.820C= NP_001341534.1:p.Leu274=
NM_001354606.1:c.820C= NP_001341535.1:p.Leu274=
NM_001354607.1:c.772C= NP_001341536.1:p.Leu258=
NM_001354608.1:c.667C= NP_001341537.1:p.Leu223=
NM_001184967.2:c.667C= NP_001171896.1:p.Leu223=
NM_001354604.2:c.823C= MANE Select NP_001341533.1:p.Leu275=
NM_001354605.2:c.820C= NP_001341534.1:p.Leu274=
NM_001354606.2:c.820C= NP_001341535.1:p.Leu274=
NM_001354607.2:c.772C= NP_001341536.1:p.Leu258=
NM_001354608.2:c.667C= NP_001341537.1:p.Leu223=
NM_198158.3:c.502C= NP_937801.1:p.Leu168=
NM_198159.3:c.823C= NP_937802.1:p.Leu275=
NM_198177.3:c.775C= NP_937820.1:p.Leu259=
NM_198178.3:c.334C= NP_937821.2:p.Leu112=
NM_000248.4:c.502C= MANE Plus Clinical NP_000239.1:p.Leu168=
NM_006722.3:c.820C= NP_006713.1:p.Leu274=