Canonical Allele Identifier: CA380982351

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763278T>G (hg19) ; chr11:g.62995806T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995806T>G , CM000673.2:g.62995806T>G	GRCh38
NC_000011.9:g.62763278T>G , CM000673.1:g.62763278T>G	GRCh37
NC_000011.8:g.62519854T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.899A>C MANE Select	ENSP00000337335.2:p.Asn300Thr
ENST00000311438.12:c.899A>C	ENSP00000311463.8:p.Asn300Thr
ENST00000336232.6:c.899A>C	ENSP00000337335.2:p.Asn300Thr
ENST00000430500.6:c.899A>C	ENSP00000398548.2:p.Asn300Thr
ENST00000535878.5:c.530A>C	ENSP00000443368.1:p.Asn177Thr
ENST00000539841.1:n.926A>C
ENST00000545207.5:c.626A>C	ENSP00000441658.1:p.Asn209Thr
NM_001184732.1:c.899A>C	NP_001171661.1:p.Asn300Thr
NM_001184733.1:c.626A>C	NP_001171662.1:p.Asn209Thr
NM_001184736.1:c.530A>C	NP_001171665.1:p.Asn177Thr
NM_004254.3:c.899A>C	NP_004245.2:p.Asn300Thr
XM_011545364.1:c.530A>C	XP_011543666.1:p.Asn177Thr
NM_004254.4:c.899A>C MANE Select	NP_004245.2:p.Asn300Thr
NM_001184732.2:c.899A>C	NP_001171661.1:p.Asn300Thr
NM_001184733.2:c.626A>C	NP_001171662.1:p.Asn209Thr
NM_001184736.2:c.530A>C	NP_001171665.1:p.Asn177Thr