Canonical Allele Identifier: CA353561810

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70005662A>G (hg19) ; chr3:g.69956511A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69956511A>G , CM000665.2:g.69956511A>G	GRCh38
NC_000003.11:g.70005662A>G , CM000665.1:g.70005662A>G	GRCh37
NC_000003.10:g.70088352A>G	NCBI36
NG_011631.1:g.222030A>G , LRG_776:g.222030A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.946A>G	ENSP00000324443.5:p.Ile316Val
ENST00000687384.1:c.943A>G	ENSP00000510225.1:p.Ile315Val
ENST00000689390.1:n.1168A>G
ENST00000693031.1:c.919A>G	ENSP00000509845.1:p.Ile307Val
ENST00000693549.1:c.946A>G	ENSP00000509358.1:p.Ile316Val
ENST00000314589.10:c.946A>G	ENSP00000324443.5:p.Ile316Val
ENST00000352241.9:c.1012A>G MANE Select	ENSP00000295600.8:p.Ile338Val
ENST00000394351.9:c.691A>G MANE Plus Clinical	ENSP00000377880.3:p.Ile231Val
ENST00000448226.9:c.991A>G	ENSP00000391803.3:p.Ile331Val
ENST00000642352.1:c.994A>G	ENSP00000494105.1:p.Ile332Val
ENST00000314557.10:c.673A>G	ENSP00000324246.6:p.Ile225Val
ENST00000314589.9:c.946A>G	ENSP00000324443.5:p.Ile316Val
ENST00000328528.10:c.991A>G	ENSP00000327867.6:p.Ile331Val
ENST00000352241.8:c.994A>G	ENSP00000295600.7:p.Ile332Val
ENST00000394351.7:c.691A>G	ENSP00000377880.3:p.Ile231Val
ENST00000448226.6:c.1012A>G	ENSP00000391803.2:p.Ile338Val
ENST00000451708.5:c.964A>G	ENSP00000398639.1:p.Ile322Val
ENST00000472437.5:c.838A>G	ENSP00000418845.1:p.Ile280Val
ENST00000478490.5:c.*338A>G	ENSP00000433487.1:n.*338A>G
ENST00000531774.1:c.505A>G	ENSP00000435909.1:p.Ile169Val
NM_000248.3:c.691A>G , LRG_776t1:c.691A>G	NP_000239.1:p.Ile231Val
NM_001184967.1:c.838A>G	NP_001171896.1:p.Ile280Val
NM_006722.2:c.991A>G	NP_006713.1:p.Ile331Val
NM_198158.2:c.673A>G	NP_937801.1:p.Ile225Val
NM_198159.2:c.994A>G	NP_937802.1:p.Ile332Val
NM_198177.2:c.946A>G	NP_937820.1:p.Ile316Val
NM_198178.2:c.505A>G	NP_937821.2:p.Ile169Val
XM_005264754.1:c.1012A>G	XP_005264811.1:p.Ile338Val
XM_005264755.2:c.964A>G	XP_005264812.1:p.Ile322Val
XM_006713164.2:c.856A>G	XP_006713227.1:p.Ile286Val
XM_011533722.1:c.1009A>G	XP_011532024.1:p.Ile337Val
XM_011533723.1:c.961A>G	XP_011532025.1:p.Ile321Val
XM_011533724.1:c.856A>G	XP_011532026.1:p.Ile286Val
XM_011533725.1:c.844A>G	XP_011532027.1:p.Ile282Val
XM_011533726.1:c.826A>G	XP_011532028.1:p.Ile276Val
NM_001354604.1:c.1012A>G	NP_001341533.1:p.Ile338Val
NM_001354605.1:c.1009A>G	NP_001341534.1:p.Ile337Val
NM_001354606.1:c.991A>G	NP_001341535.1:p.Ile331Val
NM_001354607.1:c.943A>G	NP_001341536.1:p.Ile315Val
NM_001354608.1:c.838A>G	NP_001341537.1:p.Ile280Val
NM_001184967.2:c.838A>G	NP_001171896.1:p.Ile280Val
NM_001354604.2:c.1012A>G MANE Select	NP_001341533.1:p.Ile338Val
NM_001354605.2:c.1009A>G	NP_001341534.1:p.Ile337Val
NM_001354606.2:c.991A>G	NP_001341535.1:p.Ile331Val
NM_001354607.2:c.943A>G	NP_001341536.1:p.Ile315Val
NM_001354608.2:c.838A>G	NP_001341537.1:p.Ile280Val
NM_198158.3:c.673A>G	NP_937801.1:p.Ile225Val
NM_198159.3:c.994A>G	NP_937802.1:p.Ile332Val
NM_198177.3:c.946A>G	NP_937820.1:p.Ile316Val
NM_198178.3:c.505A>G	NP_937821.2:p.Ile169Val
NM_000248.4:c.691A>G MANE Plus Clinical	NP_000239.1:p.Ile231Val
NM_006722.3:c.991A>G	NP_006713.1:p.Ile331Val