Canonical Allele Identifier: CA1978013183

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996041C= , CM000673.2:g.62996041C=	GRCh38
NC_000011.9:g.62763513C= , CM000673.1:g.62763513C=	GRCh37
NC_000011.8:g.62520089C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.873G= MANE Select	ENSP00000337335.2:p.Arg291=
ENST00000311438.12:c.873G=	ENSP00000311463.8:p.Arg291=
ENST00000336232.6:c.873G=	ENSP00000337335.2:p.Arg291=
ENST00000430500.6:c.873G=	ENSP00000398548.2:p.Arg291=
ENST00000535878.5:c.504G=	ENSP00000443368.1:p.Arg168=
ENST00000539841.1:n.691G=
ENST00000545207.5:c.600G=	ENSP00000441658.1:p.Arg200=
NM_001184732.1:c.873G=	NP_001171661.1:p.Arg291=
NM_001184733.1:c.600G=	NP_001171662.1:p.Arg200=
NM_001184736.1:c.504G=	NP_001171665.1:p.Arg168=
NM_004254.3:c.873G=	NP_004245.2:p.Arg291=
XM_011545364.1:c.504G=	XP_011543666.1:p.Arg168=
NM_004254.4:c.873G= MANE Select	NP_004245.2:p.Arg291=
NM_001184732.2:c.873G=	NP_001171661.1:p.Arg291=
NM_001184733.2:c.600G=	NP_001171662.1:p.Arg200=
NM_001184736.2:c.504G=	NP_001171665.1:p.Arg168=