Canonical Allele Identifier: CA474857641

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62766554T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999082T>C , CM000673.2:g.62999082T>C	GRCh38
NC_000011.9:g.62766554T>C , CM000673.1:g.62766554T>C	GRCh37
NC_000011.8:g.62523130T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.600A>G MANE Select	ENSP00000337335.2:p.Glu200=
ENST00000311438.12:c.600A>G	ENSP00000311463.8:p.Glu200=
ENST00000336232.6:c.600A>G	ENSP00000337335.2:p.Glu200=
ENST00000430500.6:c.600A>G	ENSP00000398548.2:p.Glu200=
ENST00000535878.5:c.231A>G	ENSP00000443368.1:p.Glu77=
ENST00000539841.1:n.418A>G
ENST00000542795.5:n.321A>G
ENST00000542904.1:n.440A>G
ENST00000545207.5:c.327A>G	ENSP00000441658.1:p.Glu109=
NM_001184732.1:c.600A>G	NP_001171661.1:p.Glu200=
NM_001184733.1:c.327A>G	NP_001171662.1:p.Glu109=
NM_001184736.1:c.231A>G	NP_001171665.1:p.Glu77=
NM_004254.3:c.600A>G	NP_004245.2:p.Glu200=
XM_011545364.1:c.231A>G	XP_011543666.1:p.Glu77=
NM_004254.4:c.600A>G MANE Select	NP_004245.2:p.Glu200=
NM_001184732.2:c.600A>G	NP_001171661.1:p.Glu200=
NM_001184733.2:c.327A>G	NP_001171662.1:p.Glu109=
NM_001184736.2:c.231A>G	NP_001171665.1:p.Glu77=