Canonical Allele Identifier: CA380983942

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62998973-A-G
• MyVariant Identifiers: chr11:g.62766445A>G (hg19) ; chr11:g.62998973A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998973A>G , CM000673.2:g.62998973A>G	GRCh38
NC_000011.9:g.62766445A>G , CM000673.1:g.62766445A>G	GRCh37
NC_000011.8:g.62523021A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.709T>C MANE Select	ENSP00000337335.2:p.Trp237Arg
ENST00000311438.12:c.709T>C	ENSP00000311463.8:p.Trp237Arg
ENST00000336232.6:c.709T>C	ENSP00000337335.2:p.Trp237Arg
ENST00000430500.6:c.709T>C	ENSP00000398548.2:p.Trp237Arg
ENST00000535878.5:c.340T>C	ENSP00000443368.1:p.Trp114Arg
ENST00000539841.1:n.527T>C
ENST00000542795.5:n.430T>C
ENST00000542904.1:n.549T>C
ENST00000545207.5:c.436T>C	ENSP00000441658.1:p.Trp146Arg
NM_001184732.1:c.709T>C	NP_001171661.1:p.Trp237Arg
NM_001184733.1:c.436T>C	NP_001171662.1:p.Trp146Arg
NM_001184736.1:c.340T>C	NP_001171665.1:p.Trp114Arg
NM_004254.3:c.709T>C	NP_004245.2:p.Trp237Arg
XM_011545364.1:c.340T>C	XP_011543666.1:p.Trp114Arg
NM_004254.4:c.709T>C MANE Select	NP_004245.2:p.Trp237Arg
NM_001184732.2:c.709T>C	NP_001171661.1:p.Trp237Arg
NM_001184733.2:c.436T>C	NP_001171662.1:p.Trp146Arg
NM_001184736.2:c.340T>C	NP_001171665.1:p.Trp114Arg