Canonical Allele Identifier: CA475140558

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763214G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995742G>T , CM000673.2:g.62995742G>T	GRCh38
NC_000011.9:g.62763214G>T , CM000673.1:g.62763214G>T	GRCh37
NC_000011.8:g.62519790G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.963C>A MANE Select	ENSP00000337335.2:p.Pro321=
ENST00000311438.12:c.963C>A	ENSP00000311463.8:p.Pro321=
ENST00000336232.6:c.963C>A	ENSP00000337335.2:p.Pro321=
ENST00000430500.6:c.963C>A	ENSP00000398548.2:p.Pro321=
ENST00000535878.5:c.594C>A	ENSP00000443368.1:p.Pro198=
ENST00000539841.1:n.990C>A
ENST00000545207.5:c.690C>A	ENSP00000441658.1:p.Pro230=
NM_001184732.1:c.963C>A	NP_001171661.1:p.Pro321=
NM_001184733.1:c.690C>A	NP_001171662.1:p.Pro230=
NM_001184736.1:c.594C>A	NP_001171665.1:p.Pro198=
NM_004254.3:c.963C>A	NP_004245.2:p.Pro321=
XM_011545364.1:c.594C>A	XP_011543666.1:p.Pro198=
NM_004254.4:c.963C>A MANE Select	NP_004245.2:p.Pro321=
NM_001184732.2:c.963C>A	NP_001171661.1:p.Pro321=
NM_001184733.2:c.690C>A	NP_001171662.1:p.Pro230=
NM_001184736.2:c.594C>A	NP_001171665.1:p.Pro198=