Canonical Allele Identifier: CA77003529

Gene: MITF

Linked Data

• ClinVar Variation Id: 1196677
• ClinVar RCV Id: RCV001560236 ; RCV003771715
• dbSNP Id: rs199578956
• gnomAD v2: 3-70014325-G-A
• gnomAD v3: 3-69965174-G-A
• gnomAD v4: 3-69965174-G-A
• MyVariant Identifiers: chr3:g.70014325G>A (hg19) ; chr3:g.69965174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965174G>A , CM000665.2:g.69965174G>A	GRCh38
NC_000003.11:g.70014325G>A , CM000665.1:g.70014325G>A	GRCh37
NC_000003.10:g.70097015G>A	NCBI36
NG_011631.1:g.230693G>A , LRG_776:g.230693G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1441G>A	ENSP00000324443.5:p.Val481Met
ENST00000687384.1:c.1438G>A	ENSP00000510225.1:p.Val480Met
ENST00000689390.1:n.1663G>A
ENST00000693031.1:c.1414G>A	ENSP00000509845.1:p.Val472Met
ENST00000693549.1:c.*252G>A	ENSP00000509358.1:n.*252G>A
ENST00000314589.10:c.1441G>A	ENSP00000324443.5:p.Val481Met
ENST00000352241.9:c.1507G>A MANE Select	ENSP00000295600.8:p.Val503Met
ENST00000394351.9:c.1186G>A MANE Plus Clinical	ENSP00000377880.3:p.Val396Met
ENST00000448226.9:c.1486G>A	ENSP00000391803.3:p.Val496Met
ENST00000642352.1:c.1489G>A	ENSP00000494105.1:p.Val497Met
ENST00000314557.10:c.1168G>A	ENSP00000324246.6:p.Val390Met
ENST00000314589.9:c.1441G>A	ENSP00000324443.5:p.Val481Met
ENST00000328528.10:c.1486G>A	ENSP00000327867.6:p.Val496Met
ENST00000352241.8:c.1489G>A	ENSP00000295600.7:p.Val497Met
ENST00000394351.7:c.1186G>A	ENSP00000377880.3:p.Val396Met
ENST00000448226.6:c.1507G>A	ENSP00000391803.2:p.Val503Met
ENST00000472437.5:c.1333G>A	ENSP00000418845.1:p.Val445Met
ENST00000478490.5:c.*833G>A	ENSP00000433487.1:n.*833G>A
ENST00000531774.1:c.1000G>A	ENSP00000435909.1:p.Val334Met
NM_000248.3:c.1186G>A , LRG_776t1:c.1186G>A	NP_000239.1:p.Val396Met
NM_001184967.1:c.1333G>A	NP_001171896.1:p.Val445Met
NM_006722.2:c.1486G>A	NP_006713.1:p.Val496Met
NM_198158.2:c.1168G>A	NP_937801.1:p.Val390Met
NM_198159.2:c.1489G>A	NP_937802.1:p.Val497Met
NM_198177.2:c.1441G>A	NP_937820.1:p.Val481Met
NM_198178.2:c.1000G>A	NP_937821.2:p.Val334Met
XM_005264754.1:c.1507G>A	XP_005264811.1:p.Val503Met
XM_005264755.2:c.1459G>A	XP_005264812.1:p.Val487Met
XM_006713164.2:c.1351G>A	XP_006713227.1:p.Val451Met
XM_011533722.1:c.1504G>A	XP_011532024.1:p.Val502Met
XM_011533723.1:c.1456G>A	XP_011532025.1:p.Val486Met
XM_011533724.1:c.1351G>A	XP_011532026.1:p.Val451Met
XM_011533725.1:c.1339G>A	XP_011532027.1:p.Val447Met
XM_011533726.1:c.1321G>A	XP_011532028.1:p.Val441Met
NM_001354604.1:c.1507G>A	NP_001341533.1:p.Val503Met
NM_001354605.1:c.1504G>A	NP_001341534.1:p.Val502Met
NM_001354606.1:c.1486G>A	NP_001341535.1:p.Val496Met
NM_001354607.1:c.1438G>A	NP_001341536.1:p.Val480Met
NM_001354608.1:c.1333G>A	NP_001341537.1:p.Val445Met
NM_001184967.2:c.1333G>A	NP_001171896.1:p.Val445Met
NM_001354604.2:c.1507G>A MANE Select	NP_001341533.1:p.Val503Met
NM_001354605.2:c.1504G>A	NP_001341534.1:p.Val502Met
NM_001354606.2:c.1486G>A	NP_001341535.1:p.Val496Met
NM_001354607.2:c.1438G>A	NP_001341536.1:p.Val480Met
NM_001354608.2:c.1333G>A	NP_001341537.1:p.Val445Met
NM_198158.3:c.1168G>A	NP_937801.1:p.Val390Met
NM_198159.3:c.1489G>A	NP_937802.1:p.Val497Met
NM_198177.3:c.1441G>A	NP_937820.1:p.Val481Met
NM_198178.3:c.1000G>A	NP_937821.2:p.Val334Met
NM_000248.4:c.1186G>A MANE Plus Clinical	NP_000239.1:p.Val396Met
NM_006722.3:c.1486G>A	NP_006713.1:p.Val496Met