Canonical Allele Identifier: CA475140530

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763196G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995724G>C , CM000673.2:g.62995724G>C	GRCh38
NC_000011.9:g.62763196G>C , CM000673.1:g.62763196G>C	GRCh37
NC_000011.8:g.62519772G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.981C>G MANE Select	ENSP00000337335.2:p.Thr327=
ENST00000311438.12:c.981C>G	ENSP00000311463.8:p.Thr327=
ENST00000336232.6:c.981C>G	ENSP00000337335.2:p.Thr327=
ENST00000430500.6:c.981C>G	ENSP00000398548.2:p.Thr327=
ENST00000535878.5:c.612C>G	ENSP00000443368.1:p.Thr204=
ENST00000539841.1:n.1008C>G
ENST00000545207.5:c.708C>G	ENSP00000441658.1:p.Thr236=
NM_001184732.1:c.981C>G	NP_001171661.1:p.Thr327=
NM_001184733.1:c.708C>G	NP_001171662.1:p.Thr236=
NM_001184736.1:c.612C>G	NP_001171665.1:p.Thr204=
NM_004254.3:c.981C>G	NP_004245.2:p.Thr327=
XM_011545364.1:c.612C>G	XP_011543666.1:p.Thr204=
NM_004254.4:c.981C>G MANE Select	NP_004245.2:p.Thr327=
NM_001184732.2:c.981C>G	NP_001171661.1:p.Thr327=
NM_001184733.2:c.708C>G	NP_001171662.1:p.Thr236=
NM_001184736.2:c.612C>G	NP_001171665.1:p.Thr204=