Canonical Allele Identifier: CA2195940765

Gene: SLCO3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92114075G= , CM000677.2:g.92114075G=	GRCh38
NC_000015.9:g.92657305G= , CM000677.1:g.92657305G=	GRCh37
NC_000015.8:g.90458309G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318445.11:c.1010-6390G= MANE Select	ENSP00000320634.6:n.1010-6390G=
ENST00000318445.10:c.1010-6390G=	ENSP00000320634.6:n.1010-6390G=
ENST00000424469.2:c.1010-6390G=	ENSP00000387846.2:n.1010-6390G=
ENST00000553653.5:n.1196-6390G=
ENST00000555549.5:n.558-6390G=
ENST00000555769.5:n.905-6390G=
NM_001145044.1:c.1010-6390G=	NP_001138516.1:n.1010-6390G=
NM_013272.3:c.1010-6390G=	NP_037404.2:n.1010-6390G=
XM_005254889.1:c.1010-6390G=	XP_005254946.1:n.1010-6390G=
XM_005254891.1:c.665-6390G=	XP_005254948.1:n.665-6390G=
XM_011521456.1:c.836-6390G=	XP_011519758.1:n.836-6390G=
XM_011521457.1:c.1010-6390G=	XP_011519759.1:n.1010-6390G=
XR_429450.2:n.930-6390G=
XR_931795.1:n.1100-6390G=
XR_931796.1:n.1100-6390G=
NR_135775.1:n.941-6390G=
XM_005254891.3:c.665-6390G=	XP_005254948.1:n.665-6390G=
XM_011521456.2:c.836-6390G=	XP_011519758.1:n.836-6390G=
XR_931796.2:n.1100-6390G=
NM_013272.4:c.1010-6390G= MANE Select	NP_037404.2:n.1010-6390G=
NR_135775.2:n.937-6390G=