Canonical Allele Identifier: CA1629084210

Gene: GSTA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52984432G= , CM000668.2:g.52984432G=	GRCh38
NC_000006.11:g.52849230G= , CM000668.1:g.52849230G=	GRCh37
NC_000006.10:g.52957189G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370963.9:c.414+32C= MANE Select	ENSP00000360002.4:n.414+32C=
ENST00000370959.1:c.414+32C=	ENSP00000359998.1:n.414+32C=
ENST00000370960.5:c.135+32C=	ENSP00000359999.1:n.135+32C=
ENST00000370963.8:c.414+32C=	ENSP00000360002.4:n.414+32C=
ENST00000457564.1:c.135+32C=	ENSP00000394228.1:n.135+32C=
ENST00000477599.5:n.355+32C=
ENST00000486559.5:n.921+32C=
NM_001512.3:c.414+32C=	NP_001503.1:n.414+32C=
XM_005249035.2:c.414+32C=	XP_005249092.1:n.414+32C=
XM_011514534.1:c.303+32C=	XP_011512836.1:n.303+32C=
XM_011514535.1:c.303+32C=	XP_011512837.1:n.303+32C=
XM_005249035.4:c.414+32C=	XP_005249092.1:n.414+32C=
XM_011514534.3:c.303+32C=	XP_011512836.1:n.303+32C=
XM_011514535.3:c.303+32C=	XP_011512837.1:n.303+32C=
NM_001512.4:c.414+32C= MANE Select	NP_001503.1:n.414+32C=