Canonical Allele Identifier: CA223625937

Gene: SLC22A8

Linked Data

• dbSNP Id: rs754480426
• gnomAD v4: 11-62999086-A-T
• MyVariant Identifiers: chr11:g.62766558A>T (hg19) ; chr11:g.62999086A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999086A>T , CM000673.2:g.62999086A>T	GRCh38
NC_000011.9:g.62766558A>T , CM000673.1:g.62766558A>T	GRCh37
NC_000011.8:g.62523134A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.596T>A MANE Select	ENSP00000337335.2:p.Val199Glu
ENST00000311438.12:c.596T>A	ENSP00000311463.8:p.Val199Glu
ENST00000336232.6:c.596T>A	ENSP00000337335.2:p.Val199Glu
ENST00000430500.6:c.596T>A	ENSP00000398548.2:p.Val199Glu
ENST00000535878.5:c.227T>A	ENSP00000443368.1:p.Val76Glu
ENST00000539841.1:n.414T>A
ENST00000542795.5:n.317T>A
ENST00000542904.1:n.436T>A
ENST00000545207.5:c.323T>A	ENSP00000441658.1:p.Val108Glu
NM_001184732.1:c.596T>A	NP_001171661.1:p.Val199Glu
NM_001184733.1:c.323T>A	NP_001171662.1:p.Val108Glu
NM_001184736.1:c.227T>A	NP_001171665.1:p.Val76Glu
NM_004254.3:c.596T>A	NP_004245.2:p.Val199Glu
XM_011545364.1:c.227T>A	XP_011543666.1:p.Val76Glu
NM_004254.4:c.596T>A MANE Select	NP_004245.2:p.Val199Glu
NM_001184732.2:c.596T>A	NP_001171661.1:p.Val199Glu
NM_001184733.2:c.323T>A	NP_001171662.1:p.Val108Glu
NM_001184736.2:c.227T>A	NP_001171665.1:p.Val76Glu