Canonical Allele Identifier: CA2195936198

Gene: SLCO3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92104415G= , CM000677.2:g.92104415G=	GRCh38
NC_000015.9:g.92647645G= , CM000677.1:g.92647645G=	GRCh37
NC_000015.8:g.90448649G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_013272.4:c.882G= MANE Select	NP_037404.2:p.Glu294=
ENST00000318445.11:c.882G= MANE Select	ENSP00000320634.6:p.Glu294=
NM_001145044.1:c.882G=	NP_001138516.1:p.Glu294=
NM_013272.3:c.882G=	NP_037404.2:p.Glu294=
NR_135775.1:n.813G=
NR_135775.2:n.809G=
ENST00000318445.10:c.882G=	ENSP00000320634.6:p.Glu294=
ENST00000424469.2:c.882G=	ENSP00000387846.2:p.Glu294=
ENST00000553653.5:n.1068G=
ENST00000555549.5:n.430G=
ENST00000555769.5:n.777G=
ENST00000556649.1:n.495G=
XM_005254889.1:c.882G=	XP_005254946.1:p.Glu294=
XM_005254891.1:c.537G=	XP_005254948.1:p.Glu179=
XM_005254891.3:c.537G=	XP_005254948.1:p.Glu179=
XM_011521456.1:c.708G=	XP_011519758.1:p.Glu236=
XM_011521456.2:c.708G=	XP_011519758.1:p.Glu236=
XM_011521457.1:c.882G=	XP_011519759.1:p.Glu294=
XR_429450.2:n.802G=
XR_931795.1:n.972G=
XR_931796.1:n.972G=
XR_931796.2:n.972G=