Canonical Allele Identifier: CA2841659798

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998832A>T , CM000673.2:g.62998832A>T	GRCh38
NC_000011.9:g.62766304A>T , CM000673.1:g.62766304A>T	GRCh37
NC_000011.8:g.62522880A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.761+89T>A MANE Select	ENSP00000337335.2:n.761+89T>A
ENST00000311438.12:c.761+89T>A	ENSP00000311463.8:n.761+89T>A
ENST00000336232.6:c.761+89T>A	ENSP00000337335.2:n.761+89T>A
ENST00000430500.6:c.761+89T>A	ENSP00000398548.2:n.761+89T>A
ENST00000535878.5:c.392+89T>A	ENSP00000443368.1:n.392+89T>A
ENST00000539841.1:n.579+89T>A
ENST00000542795.5:n.482+89T>A
ENST00000542904.1:n.601+89T>A
ENST00000545207.5:c.488+89T>A	ENSP00000441658.1:n.488+89T>A
NM_001184732.1:c.761+89T>A	NP_001171661.1:n.761+89T>A
NM_001184733.1:c.488+89T>A	NP_001171662.1:n.488+89T>A
NM_001184736.1:c.392+89T>A	NP_001171665.1:n.392+89T>A
NM_004254.3:c.761+89T>A	NP_004245.2:n.761+89T>A
XM_011545364.1:c.392+89T>A	XP_011543666.1:n.392+89T>A
NM_004254.4:c.761+89T>A MANE Select	NP_004245.2:n.761+89T>A
NM_001184732.2:c.761+89T>A	NP_001171661.1:n.761+89T>A
NM_001184733.2:c.488+89T>A	NP_001171662.1:n.488+89T>A
NM_001184736.2:c.392+89T>A	NP_001171665.1:n.392+89T>A