Canonical Allele Identifier: CA434433388

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014042A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964891A>C , CM000665.2:g.69964891A>C	GRCh38
NC_000003.11:g.70014042A>C , CM000665.1:g.70014042A>C	GRCh37
NC_000003.10:g.70096732A>C	NCBI36
NG_011631.1:g.230410A>C , LRG_776:g.230410A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000314589.11:c.1158A>C	ENSP00000324443.5:p.Pro386=
ENST00000687384.1:c.1155A>C	ENSP00000510225.1:p.Pro385=
ENST00000689390.1:n.1380A>C
ENST00000693031.1:c.1131A>C	ENSP00000509845.1:p.Pro377=
ENST00000693549.1:c.1114-23A>C	ENSP00000509358.1:n.1114-23A>C
ENST00000314589.10:c.1158A>C	ENSP00000324443.5:p.Pro386=
ENST00000352241.9:c.1224A>C MANE Select	ENSP00000295600.8:p.Pro408=
ENST00000394351.9:c.903A>C MANE Plus Clinical	ENSP00000377880.3:p.Pro301=
ENST00000448226.9:c.1203A>C	ENSP00000391803.3:p.Pro401=
ENST00000642352.1:c.1206A>C	ENSP00000494105.1:p.Pro402=
ENST00000314557.10:c.885A>C	ENSP00000324246.6:p.Pro295=
ENST00000314589.9:c.1158A>C	ENSP00000324443.5:p.Pro386=
ENST00000328528.10:c.1203A>C	ENSP00000327867.6:p.Pro401=
ENST00000352241.8:c.1206A>C	ENSP00000295600.7:p.Pro402=
ENST00000394351.7:c.903A>C	ENSP00000377880.3:p.Pro301=
ENST00000448226.6:c.1224A>C	ENSP00000391803.2:p.Pro408=
ENST00000472437.5:c.1050A>C	ENSP00000418845.1:p.Pro350=
ENST00000478490.5:c.*550A>C	ENSP00000433487.1:n.*550A>C
ENST00000531774.1:c.717A>C	ENSP00000435909.1:p.Pro239=
NM_000248.3:c.903A>C , LRG_776t1:c.903A>C	NP_000239.1:p.Pro301=
NM_001184967.1:c.1050A>C	NP_001171896.1:p.Pro350=
NM_006722.2:c.1203A>C	NP_006713.1:p.Pro401=
NM_198158.2:c.885A>C	NP_937801.1:p.Pro295=
NM_198159.2:c.1206A>C	NP_937802.1:p.Pro402=
NM_198177.2:c.1158A>C	NP_937820.1:p.Pro386=
NM_198178.2:c.717A>C	NP_937821.2:p.Pro239=
XM_005264754.1:c.1224A>C	XP_005264811.1:p.Pro408=
XM_005264755.2:c.1176A>C	XP_005264812.1:p.Pro392=
XM_006713164.2:c.1068A>C	XP_006713227.1:p.Pro356=
XM_011533722.1:c.1221A>C	XP_011532024.1:p.Pro407=
XM_011533723.1:c.1173A>C	XP_011532025.1:p.Pro391=
XM_011533724.1:c.1068A>C	XP_011532026.1:p.Pro356=
XM_011533725.1:c.1056A>C	XP_011532027.1:p.Pro352=
XM_011533726.1:c.1038A>C	XP_011532028.1:p.Pro346=
NM_001354604.1:c.1224A>C	NP_001341533.1:p.Pro408=
NM_001354605.1:c.1221A>C	NP_001341534.1:p.Pro407=
NM_001354606.1:c.1203A>C	NP_001341535.1:p.Pro401=
NM_001354607.1:c.1155A>C	NP_001341536.1:p.Pro385=
NM_001354608.1:c.1050A>C	NP_001341537.1:p.Pro350=
NM_001184967.2:c.1050A>C	NP_001171896.1:p.Pro350=
NM_001354604.2:c.1224A>C MANE Select	NP_001341533.1:p.Pro408=
NM_001354605.2:c.1221A>C	NP_001341534.1:p.Pro407=
NM_001354606.2:c.1203A>C	NP_001341535.1:p.Pro401=
NM_001354607.2:c.1155A>C	NP_001341536.1:p.Pro385=
NM_001354608.2:c.1050A>C	NP_001341537.1:p.Pro350=
NM_198158.3:c.885A>C	NP_937801.1:p.Pro295=
NM_198159.3:c.1206A>C	NP_937802.1:p.Pro402=
NM_198177.3:c.1158A>C	NP_937820.1:p.Pro386=
NM_198178.3:c.717A>C	NP_937821.2:p.Pro239=
NM_000248.4:c.903A>C MANE Plus Clinical	NP_000239.1:p.Pro301=
NM_006722.3:c.1203A>C	NP_006713.1:p.Pro401=