Canonical Allele Identifier: CA434433390

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014045C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964894C>A , CM000665.2:g.69964894C>A	GRCh38
NC_000003.11:g.70014045C>A , CM000665.1:g.70014045C>A	GRCh37
NC_000003.10:g.70096735C>A	NCBI36
NG_011631.1:g.230413C>A , LRG_776:g.230413C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314589.11:c.1161C>A	ENSP00000324443.5:p.Ser387=
ENST00000687384.1:c.1158C>A	ENSP00000510225.1:p.Ser386=
ENST00000689390.1:n.1383C>A
ENST00000693031.1:c.1134C>A	ENSP00000509845.1:p.Ser378=
ENST00000693549.1:c.1114-20C>A	ENSP00000509358.1:n.1114-20C>A
ENST00000314589.10:c.1161C>A	ENSP00000324443.5:p.Ser387=
ENST00000352241.9:c.1227C>A MANE Select	ENSP00000295600.8:p.Ser409=
ENST00000394351.9:c.906C>A MANE Plus Clinical	ENSP00000377880.3:p.Ser302=
ENST00000448226.9:c.1206C>A	ENSP00000391803.3:p.Ser402=
ENST00000642352.1:c.1209C>A	ENSP00000494105.1:p.Ser403=
ENST00000314557.10:c.888C>A	ENSP00000324246.6:p.Ser296=
ENST00000314589.9:c.1161C>A	ENSP00000324443.5:p.Ser387=
ENST00000328528.10:c.1206C>A	ENSP00000327867.6:p.Ser402=
ENST00000352241.8:c.1209C>A	ENSP00000295600.7:p.Ser403=
ENST00000394351.7:c.906C>A	ENSP00000377880.3:p.Ser302=
ENST00000448226.6:c.1227C>A	ENSP00000391803.2:p.Ser409=
ENST00000472437.5:c.1053C>A	ENSP00000418845.1:p.Ser351=
ENST00000478490.5:c.*553C>A	ENSP00000433487.1:n.*553C>A
ENST00000531774.1:c.720C>A	ENSP00000435909.1:p.Ser240=
NM_000248.3:c.906C>A , LRG_776t1:c.906C>A	NP_000239.1:p.Ser302=
NM_001184967.1:c.1053C>A	NP_001171896.1:p.Ser351=
NM_006722.2:c.1206C>A	NP_006713.1:p.Ser402=
NM_198158.2:c.888C>A	NP_937801.1:p.Ser296=
NM_198159.2:c.1209C>A	NP_937802.1:p.Ser403=
NM_198177.2:c.1161C>A	NP_937820.1:p.Ser387=
NM_198178.2:c.720C>A	NP_937821.2:p.Ser240=
XM_005264754.1:c.1227C>A	XP_005264811.1:p.Ser409=
XM_005264755.2:c.1179C>A	XP_005264812.1:p.Ser393=
XM_006713164.2:c.1071C>A	XP_006713227.1:p.Ser357=
XM_011533722.1:c.1224C>A	XP_011532024.1:p.Ser408=
XM_011533723.1:c.1176C>A	XP_011532025.1:p.Ser392=
XM_011533724.1:c.1071C>A	XP_011532026.1:p.Ser357=
XM_011533725.1:c.1059C>A	XP_011532027.1:p.Ser353=
XM_011533726.1:c.1041C>A	XP_011532028.1:p.Ser347=
NM_001354604.1:c.1227C>A	NP_001341533.1:p.Ser409=
NM_001354605.1:c.1224C>A	NP_001341534.1:p.Ser408=
NM_001354606.1:c.1206C>A	NP_001341535.1:p.Ser402=
NM_001354607.1:c.1158C>A	NP_001341536.1:p.Ser386=
NM_001354608.1:c.1053C>A	NP_001341537.1:p.Ser351=
NM_001184967.2:c.1053C>A	NP_001171896.1:p.Ser351=
NM_001354604.2:c.1227C>A MANE Select	NP_001341533.1:p.Ser409=
NM_001354605.2:c.1224C>A	NP_001341534.1:p.Ser408=
NM_001354606.2:c.1206C>A	NP_001341535.1:p.Ser402=
NM_001354607.2:c.1158C>A	NP_001341536.1:p.Ser386=
NM_001354608.2:c.1053C>A	NP_001341537.1:p.Ser351=
NM_198158.3:c.888C>A	NP_937801.1:p.Ser296=
NM_198159.3:c.1209C>A	NP_937802.1:p.Ser403=
NM_198177.3:c.1161C>A	NP_937820.1:p.Ser387=
NM_198178.3:c.720C>A	NP_937821.2:p.Ser240=
NM_000248.4:c.906C>A MANE Plus Clinical	NP_000239.1:p.Ser302=
NM_006722.3:c.1206C>A	NP_006713.1:p.Ser402=