Canonical Allele Identifier: CA2195887449

Gene: SLCO3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92008779A= , CM000677.2:g.92008779A=	GRCh38
NC_000015.9:g.92552009A= , CM000677.1:g.92552009A=	GRCh37
NC_000015.8:g.90353013A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318445.11:c.647-86102A= MANE Select	ENSP00000320634.6:n.647-86102A=
ENST00000318445.10:c.647-86102A=	ENSP00000320634.6:n.647-86102A=
ENST00000424469.2:c.647-86102A=	ENSP00000387846.2:n.647-86102A=
ENST00000553653.5:n.833-86102A=
ENST00000555769.5:n.542-86102A=
ENST00000556649.1:n.259+67203A=
NM_001145044.1:c.647-86102A=	NP_001138516.1:n.647-86102A=
NM_013272.3:c.647-86102A=	NP_037404.2:n.647-86102A=
XM_005254889.1:c.647-86102A=	XP_005254946.1:n.647-86102A=
XM_005254891.1:c.302-86102A=	XP_005254948.1:n.302-86102A=
XM_011521456.1:c.473-86102A=	XP_011519758.1:n.473-86102A=
XM_011521457.1:c.647-86102A=	XP_011519759.1:n.647-86102A=
XR_429450.2:n.567-86102A=
XR_931795.1:n.737-86102A=
XR_931796.1:n.737-86102A=
NR_135775.1:n.578-86102A=
XM_005254891.3:c.302-86102A=	XP_005254948.1:n.302-86102A=
XM_011521456.2:c.473-86102A=	XP_011519758.1:n.473-86102A=
XR_931796.2:n.737-86102A=
NM_013272.4:c.647-86102A= MANE Select	NP_037404.2:n.647-86102A=
NR_135775.2:n.574-86102A=