Canonical Allele Identifier: CA2574853430

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998874_62998875insTGC , CM000673.2:g.62998874_62998875insTGC	GRCh38
NC_000011.9:g.62766346_62766347insTGC , CM000673.1:g.62766346_62766347insTGC	GRCh37
NC_000011.8:g.62522922_62522923insTGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.761+46_761+47insGCA MANE Select	ENSP00000337335.2:n.761+46_761+47insGCA
ENST00000311438.12:c.761+46_761+47insGCA	ENSP00000311463.8:n.761+46_761+47insGCA
ENST00000336232.6:c.761+46_761+47insGCA	ENSP00000337335.2:n.761+46_761+47insGCA
ENST00000430500.6:c.761+46_761+47insGCA	ENSP00000398548.2:n.761+46_761+47insGCA
ENST00000535878.5:c.392+46_392+47insGCA	ENSP00000443368.1:n.392+46_392+47insGCA
ENST00000539841.1:n.579+46_579+47insGCA
ENST00000542795.5:n.482+46_482+47insGCA
ENST00000542904.1:n.601+46_601+47insGCA
ENST00000545207.5:c.488+46_488+47insGCA	ENSP00000441658.1:n.488+46_488+47insGCA
NM_001184732.1:c.761+46_761+47insGCA	NP_001171661.1:n.761+46_761+47insGCA
NM_001184733.1:c.488+46_488+47insGCA	NP_001171662.1:n.488+46_488+47insGCA
NM_001184736.1:c.392+46_392+47insGCA	NP_001171665.1:n.392+46_392+47insGCA
NM_004254.3:c.761+46_761+47insGCA	NP_004245.2:n.761+46_761+47insGCA
XM_011545364.1:c.392+46_392+47insGCA	XP_011543666.1:n.392+46_392+47insGCA
NM_004254.4:c.761+46_761+47insGCA MANE Select	NP_004245.2:n.761+46_761+47insGCA
NM_001184732.2:c.761+46_761+47insGCA	NP_001171661.1:n.761+46_761+47insGCA
NM_001184733.2:c.488+46_488+47insGCA	NP_001171662.1:n.488+46_488+47insGCA
NM_001184736.2:c.392+46_392+47insGCA	NP_001171665.1:n.392+46_392+47insGCA