Canonical Allele Identifier: CA474857677

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62999088-A-G
• MyVariant Identifiers: chr11:g.62766560A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999088A>G , CM000673.2:g.62999088A>G	GRCh38
NC_000011.9:g.62766560A>G , CM000673.1:g.62766560A>G	GRCh37
NC_000011.8:g.62523136A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.594T>C MANE Select	ENSP00000337335.2:p.Asn198=
ENST00000311438.12:c.594T>C	ENSP00000311463.8:p.Asn198=
ENST00000336232.6:c.594T>C	ENSP00000337335.2:p.Asn198=
ENST00000430500.6:c.594T>C	ENSP00000398548.2:p.Asn198=
ENST00000535878.5:c.225T>C	ENSP00000443368.1:p.Asn75=
ENST00000539841.1:n.412T>C
ENST00000542795.5:n.315T>C
ENST00000542904.1:n.434T>C
ENST00000545207.5:c.321T>C	ENSP00000441658.1:p.Asn107=
NM_001184732.1:c.594T>C	NP_001171661.1:p.Asn198=
NM_001184733.1:c.321T>C	NP_001171662.1:p.Asn107=
NM_001184736.1:c.225T>C	NP_001171665.1:p.Asn75=
NM_004254.3:c.594T>C	NP_004245.2:p.Asn198=
XM_011545364.1:c.225T>C	XP_011543666.1:p.Asn75=
NM_004254.4:c.594T>C MANE Select	NP_004245.2:p.Asn198=
NM_001184732.2:c.594T>C	NP_001171661.1:p.Asn198=
NM_001184733.2:c.321T>C	NP_001171662.1:p.Asn107=
NM_001184736.2:c.225T>C	NP_001171665.1:p.Asn75=