Canonical Allele Identifier: CA1978016065

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999087C= , CM000673.2:g.62999087C=	GRCh38
NC_000011.9:g.62766559C= , CM000673.1:g.62766559C=	GRCh37
NC_000011.8:g.62523135C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.595G= MANE Select	ENSP00000337335.2:p.Val199=
ENST00000311438.12:c.595G=	ENSP00000311463.8:p.Val199=
ENST00000336232.6:c.595G=	ENSP00000337335.2:p.Val199=
ENST00000430500.6:c.595G=	ENSP00000398548.2:p.Val199=
ENST00000535878.5:c.226G=	ENSP00000443368.1:p.Val76=
ENST00000539841.1:n.413G=
ENST00000542795.5:n.316G=
ENST00000542904.1:n.435G=
ENST00000545207.5:c.322G=	ENSP00000441658.1:p.Val108=
NM_001184732.1:c.595G=	NP_001171661.1:p.Val199=
NM_001184733.1:c.322G=	NP_001171662.1:p.Val108=
NM_001184736.1:c.226G=	NP_001171665.1:p.Val76=
NM_004254.3:c.595G=	NP_004245.2:p.Val199=
XM_011545364.1:c.226G=	XP_011543666.1:p.Val76=
NM_004254.4:c.595G= MANE Select	NP_004245.2:p.Val199=
NM_001184732.2:c.595G=	NP_001171661.1:p.Val199=
NM_001184733.2:c.322G=	NP_001171662.1:p.Val108=
NM_001184736.2:c.226G=	NP_001171665.1:p.Val76=