Canonical Allele Identifier: CA475140893

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62763609G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996137G>C , CM000673.2:g.62996137G>C	GRCh38
NC_000011.9:g.62763609G>C , CM000673.1:g.62763609G>C	GRCh37
NC_000011.8:g.62520185G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.777C>G MANE Select	ENSP00000337335.2:p.Ser259=
ENST00000311438.12:c.777C>G	ENSP00000311463.8:p.Ser259=
ENST00000336232.6:c.777C>G	ENSP00000337335.2:p.Ser259=
ENST00000430500.6:c.777C>G	ENSP00000398548.2:p.Ser259=
ENST00000535878.5:c.408C>G	ENSP00000443368.1:p.Ser136=
ENST00000539841.1:n.595C>G
ENST00000542795.5:n.498C>G
ENST00000542904.1:n.617C>G
ENST00000545207.5:c.504C>G	ENSP00000441658.1:p.Ser168=
NM_001184732.1:c.777C>G	NP_001171661.1:p.Ser259=
NM_001184733.1:c.504C>G	NP_001171662.1:p.Ser168=
NM_001184736.1:c.408C>G	NP_001171665.1:p.Ser136=
NM_004254.3:c.777C>G	NP_004245.2:p.Ser259=
XM_011545364.1:c.408C>G	XP_011543666.1:p.Ser136=
NM_004254.4:c.777C>G MANE Select	NP_004245.2:p.Ser259=
NM_001184732.2:c.777C>G	NP_001171661.1:p.Ser259=
NM_001184733.2:c.504C>G	NP_001171662.1:p.Ser168=
NM_001184736.2:c.408C>G	NP_001171665.1:p.Ser136=