Canonical Allele Identifier: CA380982806

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763612C>G (hg19) ; chr11:g.62996140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996140C>G , CM000673.2:g.62996140C>G	GRCh38
NC_000011.9:g.62763612C>G , CM000673.1:g.62763612C>G	GRCh37
NC_000011.8:g.62520188C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.774G>C MANE Select	ENSP00000337335.2:p.Glu258Asp
ENST00000311438.12:c.774G>C	ENSP00000311463.8:p.Glu258Asp
ENST00000336232.6:c.774G>C	ENSP00000337335.2:p.Glu258Asp
ENST00000430500.6:c.774G>C	ENSP00000398548.2:p.Glu258Asp
ENST00000535878.5:c.405G>C	ENSP00000443368.1:p.Glu135Asp
ENST00000539841.1:n.592G>C
ENST00000542795.5:n.495G>C
ENST00000542904.1:n.614G>C
ENST00000545207.5:c.501G>C	ENSP00000441658.1:p.Glu167Asp
NM_001184732.1:c.774G>C	NP_001171661.1:p.Glu258Asp
NM_001184733.1:c.501G>C	NP_001171662.1:p.Glu167Asp
NM_001184736.1:c.405G>C	NP_001171665.1:p.Glu135Asp
NM_004254.3:c.774G>C	NP_004245.2:p.Glu258Asp
XM_011545364.1:c.405G>C	XP_011543666.1:p.Glu135Asp
NM_004254.4:c.774G>C MANE Select	NP_004245.2:p.Glu258Asp
NM_001184732.2:c.774G>C	NP_001171661.1:p.Glu258Asp
NM_001184733.2:c.501G>C	NP_001171662.1:p.Glu167Asp
NM_001184736.2:c.405G>C	NP_001171665.1:p.Glu135Asp