Canonical Allele Identifier: CA1978017062

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999835G= , CM000673.2:g.62999835G=	GRCh38
NC_000011.9:g.62767307G= , CM000673.1:g.62767307G=	GRCh37
NC_000011.8:g.62523883G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004254.4:c.445C= MANE Select	NP_004245.2:p.Arg149=
ENST00000336232.7:c.445C= MANE Select	ENSP00000337335.2:p.Arg149=
NM_001184732.1:c.445C=	NP_001171661.1:p.Arg149=
NM_001184732.2:c.445C=	NP_001171661.1:p.Arg149=
NM_001184733.1:c.172C=	NP_001171662.1:p.Arg58=
NM_001184733.2:c.172C=	NP_001171662.1:p.Arg58=
NM_001184736.1:c.76C=	NP_001171665.1:p.Arg26=
NM_001184736.2:c.76C=	NP_001171665.1:p.Arg26=
NM_004254.3:c.445C=	NP_004245.2:p.Arg149=
ENST00000311438.12:c.445C=	ENSP00000311463.8:p.Arg149=
ENST00000336232.6:c.445C=	ENSP00000337335.2:p.Arg149=
ENST00000430500.6:c.445C=	ENSP00000398548.2:p.Arg149=
ENST00000535878.5:c.76C=	ENSP00000443368.1:p.Arg26=
ENST00000542795.5:n.166C=
ENST00000542904.1:n.285C=
ENST00000545207.5:c.172C=	ENSP00000441658.1:p.Arg58=
XM_011545364.1:c.76C=	XP_011543666.1:p.Arg26=