Canonical Allele Identifier: CA475140498

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763178G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995706G>T , CM000673.2:g.62995706G>T	GRCh38
NC_000011.9:g.62763178G>T , CM000673.1:g.62763178G>T	GRCh37
NC_000011.8:g.62519754G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.999C>A MANE Select	ENSP00000337335.2:p.Ala333=
ENST00000311438.12:c.999C>A	ENSP00000311463.8:p.Ala333=
ENST00000336232.6:c.999C>A	ENSP00000337335.2:p.Ala333=
ENST00000430500.6:c.999C>A	ENSP00000398548.2:p.Ala333=
ENST00000535878.5:c.630C>A	ENSP00000443368.1:p.Ala210=
ENST00000539841.1:n.1026C>A
ENST00000545207.5:c.726C>A	ENSP00000441658.1:p.Ala242=
NM_001184732.1:c.999C>A	NP_001171661.1:p.Ala333=
NM_001184733.1:c.726C>A	NP_001171662.1:p.Ala242=
NM_001184736.1:c.630C>A	NP_001171665.1:p.Ala210=
NM_004254.3:c.999C>A	NP_004245.2:p.Ala333=
XM_011545364.1:c.630C>A	XP_011543666.1:p.Ala210=
NM_004254.4:c.999C>A MANE Select	NP_004245.2:p.Ala333=
NM_001184732.2:c.999C>A	NP_001171661.1:p.Ala333=
NM_001184733.2:c.726C>A	NP_001171662.1:p.Ala242=
NM_001184736.2:c.630C>A	NP_001171665.1:p.Ala210=