Canonical Allele Identifier: CA14124803

Gene: SLCO3A1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92142548T>C , CM000677.2:g.92142548T>C	GRCh38
NC_000015.9:g.92685778T>C , CM000677.1:g.92685778T>C	GRCh37
NC_000015.8:g.90486782T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318445.11:c.1513-4436T>C MANE Select	ENSP00000320634.6:n.1513-4436T>C
ENST00000318445.10:c.1513-4436T>C	ENSP00000320634.6:n.1513-4436T>C
ENST00000424469.2:c.1513-4436T>C	ENSP00000387846.2:n.1513-4436T>C
ENST00000553653.5:n.1699-4436T>C
ENST00000555210.1:c.214-4436T>C
ENST00000555549.5:n.1061-4436T>C
ENST00000555769.5:n.1408-4436T>C
ENST00000555892.5:c.150-4436T>C	ENSP00000451287.1:n.150-4436T>C
NM_001145044.1:c.1513-4436T>C	NP_001138516.1:n.1513-4436T>C
NM_013272.3:c.1513-4436T>C	NP_037404.2:n.1513-4436T>C
XM_005254889.1:c.1513-4436T>C	XP_005254946.1:n.1513-4436T>C
XM_005254891.1:c.1168-4436T>C	XP_005254948.1:n.1168-4436T>C
XM_011521456.1:c.1339-4436T>C	XP_011519758.1:n.1339-4436T>C
XM_011521457.1:c.1513-4436T>C	XP_011519759.1:n.1513-4436T>C
XR_429450.2:n.1433-4436T>C
XR_931795.1:n.1603-4436T>C
XR_931796.1:n.1603-4436T>C
NR_135775.1:n.1444-4436T>C
XM_005254891.3:c.1168-4436T>C	XP_005254948.1:n.1168-4436T>C
XM_011521456.2:c.1339-4436T>C	XP_011519758.1:n.1339-4436T>C
XR_931796.2:n.1603-4436T>C
NM_013272.4:c.1513-4436T>C MANE Select	NP_037404.2:n.1513-4436T>C
NR_135775.2:n.1440-4436T>C