Canonical Allele Identifier: CA77001741

Gene: MITF

Linked Data

• ClinVar Variation Id: 1305042
• ClinVar RCV Id: RCV001765217 ; RCV002540238 ; RCV003339730
• dbSNP Id: rs763339433
• gnomAD v2: 3-69998262-C-A
• gnomAD v3: 3-69949111-C-A
• gnomAD v4: 3-69949111-C-A
• MyVariant Identifiers: chr3:g.69998262C>A (hg19) ; chr3:g.69949111C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.775C>A	ENSP00000324443.5:p.Leu259Ile
ENST00000687384.1:c.772C>A	ENSP00000510225.1:p.Leu258Ile
ENST00000689390.1:n.997C>A
ENST00000693031.1:c.748C>A	ENSP00000509845.1:p.Leu250Ile
ENST00000693549.1:c.775C>A	ENSP00000509358.1:p.Leu259Ile
ENST00000314589.10:c.775C>A	ENSP00000324443.5:p.Leu259Ile
ENST00000352241.9:c.823C>A MANE Select	ENSP00000295600.8:p.Leu275Ile
ENST00000394351.9:c.502C>A MANE Plus Clinical	ENSP00000377880.3:p.Leu168Ile
ENST00000448226.9:c.820C>A	ENSP00000391803.3:p.Leu274Ile
ENST00000642352.1:c.823C>A	ENSP00000494105.1:p.Leu275Ile
ENST00000314557.10:c.502C>A	ENSP00000324246.6:p.Leu168Ile
ENST00000314589.9:c.775C>A	ENSP00000324443.5:p.Leu259Ile
ENST00000328528.10:c.820C>A	ENSP00000327867.6:p.Leu274Ile
ENST00000352241.8:c.823C>A	ENSP00000295600.7:p.Leu275Ile
ENST00000394351.7:c.502C>A	ENSP00000377880.3:p.Leu168Ile
ENST00000448226.6:c.823C>A	ENSP00000391803.2:p.Leu275Ile
ENST00000451708.5:c.775C>A	ENSP00000398639.1:p.Leu259Ile
ENST00000472437.5:c.667C>A	ENSP00000418845.1:p.Leu223Ile
ENST00000478490.5:c.*149C>A	ENSP00000433487.1:n.*149C>A
ENST00000531774.1:c.334C>A	ENSP00000435909.1:p.Leu112Ile
NM_000248.3:c.502C>A , LRG_776t1:c.502C>A	NP_000239.1:p.Leu168Ile
NM_001184967.1:c.667C>A	NP_001171896.1:p.Leu223Ile
NM_006722.2:c.820C>A	NP_006713.1:p.Leu274Ile
NM_198158.2:c.502C>A	NP_937801.1:p.Leu168Ile
NM_198159.2:c.823C>A	NP_937802.1:p.Leu275Ile
NM_198177.2:c.775C>A	NP_937820.1:p.Leu259Ile
NM_198178.2:c.334C>A	NP_937821.2:p.Leu112Ile
XM_005264754.1:c.823C>A	XP_005264811.1:p.Leu275Ile
XM_005264755.2:c.775C>A	XP_005264812.1:p.Leu259Ile
XM_006713164.2:c.667C>A	XP_006713227.1:p.Leu223Ile
XM_011533722.1:c.820C>A	XP_011532024.1:p.Leu274Ile
XM_011533723.1:c.772C>A	XP_011532025.1:p.Leu258Ile
XM_011533724.1:c.667C>A	XP_011532026.1:p.Leu223Ile
XM_011533725.1:c.655C>A	XP_011532027.1:p.Leu219Ile
XM_011533726.1:c.655C>A	XP_011532028.1:p.Leu219Ile
NM_001354604.1:c.823C>A	NP_001341533.1:p.Leu275Ile
NM_001354605.1:c.820C>A	NP_001341534.1:p.Leu274Ile
NM_001354606.1:c.820C>A	NP_001341535.1:p.Leu274Ile
NM_001354607.1:c.772C>A	NP_001341536.1:p.Leu258Ile
NM_001354608.1:c.667C>A	NP_001341537.1:p.Leu223Ile
NM_001184967.2:c.667C>A	NP_001171896.1:p.Leu223Ile
NM_001354604.2:c.823C>A MANE Select	NP_001341533.1:p.Leu275Ile
NM_001354605.2:c.820C>A	NP_001341534.1:p.Leu274Ile
NM_001354606.2:c.820C>A	NP_001341535.1:p.Leu274Ile
NM_001354607.2:c.772C>A	NP_001341536.1:p.Leu258Ile
NM_001354608.2:c.667C>A	NP_001341537.1:p.Leu223Ile
NM_198158.3:c.502C>A	NP_937801.1:p.Leu168Ile
NM_198159.3:c.823C>A	NP_937802.1:p.Leu275Ile
NM_198177.3:c.775C>A	NP_937820.1:p.Leu259Ile
NM_198178.3:c.334C>A	NP_937821.2:p.Leu112Ile
NM_000248.4:c.502C>A MANE Plus Clinical	NP_000239.1:p.Leu168Ile
NM_006722.3:c.820C>A	NP_006713.1:p.Leu274Ile