Canonical Allele Identifier: CA474857607

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62766548C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999076C>G , CM000673.2:g.62999076C>G	GRCh38
NC_000011.9:g.62766548C>G , CM000673.1:g.62766548C>G	GRCh37
NC_000011.8:g.62523124C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.606G>C MANE Select	ENSP00000337335.2:p.Val202=
ENST00000311438.12:c.606G>C	ENSP00000311463.8:p.Val202=
ENST00000336232.6:c.606G>C	ENSP00000337335.2:p.Val202=
ENST00000430500.6:c.606G>C	ENSP00000398548.2:p.Val202=
ENST00000535878.5:c.237G>C	ENSP00000443368.1:p.Val79=
ENST00000539841.1:n.424G>C
ENST00000542795.5:n.327G>C
ENST00000542904.1:n.446G>C
ENST00000545207.5:c.333G>C	ENSP00000441658.1:p.Val111=
NM_001184732.1:c.606G>C	NP_001171661.1:p.Val202=
NM_001184733.1:c.333G>C	NP_001171662.1:p.Val111=
NM_001184736.1:c.237G>C	NP_001171665.1:p.Val79=
NM_004254.3:c.606G>C	NP_004245.2:p.Val202=
XM_011545364.1:c.237G>C	XP_011543666.1:p.Val79=
NM_004254.4:c.606G>C MANE Select	NP_004245.2:p.Val202=
NM_001184732.2:c.606G>C	NP_001171661.1:p.Val202=
NM_001184733.2:c.333G>C	NP_001171662.1:p.Val111=
NM_001184736.2:c.237G>C	NP_001171665.1:p.Val79=