Canonical Allele Identifier: CA475140677

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62995808-G-GC
• MyVariant Identifiers: chr11:g.62763280_62763281insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995808_62995809insC , CM000673.2:g.62995808_62995809insC	GRCh38
NC_000011.9:g.62763280_62763281insC , CM000673.1:g.62763280_62763281insC	GRCh37
NC_000011.8:g.62519856_62519857insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.896_897insG MANE Select	ENSP00000337335.2:p.Asn300GlnfsTer17
ENST00000311438.12:c.896_897insG	ENSP00000311463.8:p.Asn300GlnfsTer17
ENST00000336232.6:c.896_897insG	ENSP00000337335.2:p.Asn300GlnfsTer17
ENST00000430500.6:c.896_897insG	ENSP00000398548.2:p.Asn300GlnfsTer17
ENST00000535878.5:c.527_528insG	ENSP00000443368.1:p.Asn177GlnfsTer17
ENST00000539841.1:n.923_924insG
ENST00000545207.5:c.623_624insG	ENSP00000441658.1:p.Asn209GlnfsTer17
NM_001184732.1:c.896_897insG	NP_001171661.1:p.Asn300GlnfsTer17
NM_001184733.1:c.623_624insG	NP_001171662.1:p.Asn209GlnfsTer17
NM_001184736.1:c.527_528insG	NP_001171665.1:p.Asn177GlnfsTer17
NM_004254.3:c.896_897insG	NP_004245.2:p.Asn300GlnfsTer17
XM_011545364.1:c.527_528insG	XP_011543666.1:p.Asn177GlnfsTer17
NM_004254.4:c.896_897insG MANE Select	NP_004245.2:p.Asn300GlnfsTer17
NM_001184732.2:c.896_897insG	NP_001171661.1:p.Asn300GlnfsTer17
NM_001184733.2:c.623_624insG	NP_001171662.1:p.Asn209GlnfsTer17
NM_001184736.2:c.527_528insG	NP_001171665.1:p.Asn177GlnfsTer17