Canonical Allele Identifier: CA1978012936

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995839_62995840delinsAG , CM000673.2:g.62995839_62995840delinsAG	GRCh38
NC_000011.9:g.62763311_62763312delinsAG , CM000673.1:g.62763311_62763312delinsAG	GRCh37
NC_000011.8:g.62519887_62519888delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.886-21_886-20delinsCT MANE Select	ENSP00000337335.2:n.886-21_886-20delinsCT
ENST00000311438.12:c.886-21_886-20delinsCT	ENSP00000311463.8:n.886-21_886-20delinsCT
ENST00000336232.6:c.886-21_886-20delinsCT	ENSP00000337335.2:n.886-21_886-20delinsCT
ENST00000430500.6:c.886-21_886-20delinsCT	ENSP00000398548.2:n.886-21_886-20delinsCT
ENST00000535878.5:c.517-21_517-20delinsCT	ENSP00000443368.1:n.517-21_517-20delinsCT
ENST00000539841.1:n.892_893delinsCT
ENST00000545207.5:c.613-21_613-20delinsCT	ENSP00000441658.1:n.613-21_613-20delinsCT
NM_001184732.1:c.886-21_886-20delinsCT	NP_001171661.1:n.886-21_886-20delinsCT
NM_001184733.1:c.613-21_613-20delinsCT	NP_001171662.1:n.613-21_613-20delinsCT
NM_001184736.1:c.517-21_517-20delinsCT	NP_001171665.1:n.517-21_517-20delinsCT
NM_004254.3:c.886-21_886-20delinsCT	NP_004245.2:n.886-21_886-20delinsCT
XM_011545364.1:c.517-21_517-20delinsCT	XP_011543666.1:n.517-21_517-20delinsCT
NM_004254.4:c.886-21_886-20delinsCT MANE Select	NP_004245.2:n.886-21_886-20delinsCT
NM_001184732.2:c.886-21_886-20delinsCT	NP_001171661.1:n.886-21_886-20delinsCT
NM_001184733.2:c.613-21_613-20delinsCT	NP_001171662.1:n.613-21_613-20delinsCT
NM_001184736.2:c.517-21_517-20delinsCT	NP_001171665.1:n.517-21_517-20delinsCT