Canonical Allele Identifier: CA1140099351

Gene: MGST3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165647351T= , CM000663.2:g.165647351T=	GRCh38
NC_000001.10:g.165616588T= , CM000663.1:g.165616588T=	GRCh37
NC_000001.9:g.163883212T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367889.8:c.-7-2490T= MANE Select	ENSP00000356864.3:n.-7-2490T=
ENST00000367883.3:c.36-2490T=	ENSP00000356858.1:n.36-2490T=
ENST00000367884.6:c.-7-2490T=	ENSP00000356859.1:n.-7-2490T=
ENST00000367885.5:c.36-2490T=	ENSP00000356860.1:n.36-2490T=
ENST00000367888.8:c.-7-2490T=	ENSP00000356863.4:n.-7-2490T=
ENST00000367889.7:c.-7-2490T=	ENSP00000356864.3:n.-7-2490T=
ENST00000461308.1:n.69-2490T=
ENST00000461759.1:n.1691T=
ENST00000488688.1:n.37-2490T=
ENST00000495447.5:n.56-2404T=
ENST00000627653.1:c.36-2490T=	ENSP00000487151.1:n.36-2490T=
NM_004528.3:c.-7-2490T=	NP_004519.1:n.-7-2490T=
XM_005245174.2:c.-7-2490T=	XP_005245231.2:n.-7-2490T=
XM_005245174.3:c.-7-2490T=	XP_005245231.2:n.-7-2490T=
NM_004528.4:c.-7-2490T= MANE Select	NP_004519.1:n.-7-2490T=