Canonical Allele Identifier: CA1978022399

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63003893C= , CM000673.2:g.63003893C=	GRCh38
NC_000011.9:g.62771365C= , CM000673.1:g.62771365C=	GRCh37
NC_000011.8:g.62527941C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.334-3070G= MANE Select	ENSP00000337335.2:n.334-3070G=
ENST00000311438.12:c.334-3070G=	ENSP00000311463.8:n.334-3070G=
ENST00000336232.6:c.334-3070G=	ENSP00000337335.2:n.334-3070G=
ENST00000430500.6:c.334-3070G=	ENSP00000398548.2:n.334-3070G=
ENST00000535878.5:c.-36-3070G=	ENSP00000443368.1:n.-36-3070G=
ENST00000545207.5:c.61-3070G=	ENSP00000441658.1:n.61-3070G=
NM_001184732.1:c.334-3070G=	NP_001171661.1:n.334-3070G=
NM_001184733.1:c.61-3070G=	NP_001171662.1:n.61-3070G=
NM_001184736.1:c.-36-3070G=	NP_001171665.1:n.-36-3070G=
NM_004254.3:c.334-3070G=	NP_004245.2:n.334-3070G=
NM_004254.4:c.334-3070G= MANE Select	NP_004245.2:n.334-3070G=
NM_001184732.2:c.334-3070G=	NP_001171661.1:n.334-3070G=
NM_001184733.2:c.61-3070G=	NP_001171662.1:n.61-3070G=
NM_001184736.2:c.-36-3070G=	NP_001171665.1:n.-36-3070G=