Canonical Allele Identifier: CA9947005

Gene: SLCO4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62657239C>T , CM000682.2:g.62657239C>T	GRCh38
NC_000020.10:g.61288591C>T , CM000682.1:g.61288591C>T	GRCh37
NC_000020.9:g.60759036C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016354.4:c.785C>T MANE Select	NP_057438.3:p.Pro262Leu
ENST00000217159.6:c.785C>T MANE Select	ENSP00000217159.1:p.Pro262Leu
NM_016354.3:c.785C>T	NP_057438.3:p.Pro262Leu
ENST00000217159.5:c.785C>T	ENSP00000217159.1:p.Pro262Leu
ENST00000370507.5:c.785C>T	ENSP00000359538.1:p.Pro262Leu
ENST00000497209.5:c.785C>T	ENSP00000434245.1:p.Pro262Leu
XM_005260203.2:c.785C>T	XP_005260260.1:p.Pro262Leu
XM_005260203.3:c.785C>T	XP_005260260.1:p.Pro262Leu
XM_011528791.1:c.785C>T	XP_011527093.1:p.Pro262Leu
XM_011528792.1:c.785C>T	XP_011527094.1:p.Pro262Leu
XM_011528792.3:c.785C>T	XP_011527094.1:p.Pro262Leu
XM_011528793.1:c.785C>T	XP_011527095.1:p.Pro262Leu
XM_011528794.1:c.785C>T	XP_011527096.1:p.Pro262Leu
XM_017027826.1:c.785C>T	XP_016883315.1:p.Pro262Leu
XM_017027827.2:c.785C>T	XP_016883316.1:p.Pro262Leu
XR_001754249.2:n.1377C>T
XR_001754250.2:n.998C>T
XR_001754251.2:n.1377C>T
XR_001754252.1:n.970C>T
XR_001754253.2:n.1377C>T
XR_001754254.2:n.1377C>T
XR_001754255.2:n.1377C>T
XR_001754256.2:n.1377C>T
XR_001754257.2:n.1377C>T
XR_001754258.2:n.1377C>T
XR_002958473.1:n.1377C>T
XR_002958474.1:n.1377C>T
XR_244115.2:n.987C>T
XR_244115.4:n.1377C>T
XR_244116.2:n.987C>T
XR_244116.4:n.1377C>T
XR_244117.2:n.987C>T
XR_936522.1:n.987C>T
XR_936523.1:n.987C>T
XR_936524.1:n.987C>T
XR_936524.2:n.1377C>T