Canonical Allele Identifier: CA1978012976

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995870G= , CM000673.2:g.62995870G=	GRCh38
NC_000011.9:g.62763342G= , CM000673.1:g.62763342G=	GRCh37
NC_000011.8:g.62519918G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.886-51C= MANE Select	ENSP00000337335.2:n.886-51C=
ENST00000311438.12:c.886-51C=	ENSP00000311463.8:n.886-51C=
ENST00000336232.6:c.886-51C=	ENSP00000337335.2:n.886-51C=
ENST00000430500.6:c.886-51C=	ENSP00000398548.2:n.886-51C=
ENST00000535878.5:c.517-51C=	ENSP00000443368.1:n.517-51C=
ENST00000539841.1:n.862C=
ENST00000545207.5:c.613-51C=	ENSP00000441658.1:n.613-51C=
NM_001184732.1:c.886-51C=	NP_001171661.1:n.886-51C=
NM_001184733.1:c.613-51C=	NP_001171662.1:n.613-51C=
NM_001184736.1:c.517-51C=	NP_001171665.1:n.517-51C=
NM_004254.3:c.886-51C=	NP_004245.2:n.886-51C=
XM_011545364.1:c.517-51C=	XP_011543666.1:n.517-51C=
NM_004254.4:c.886-51C= MANE Select	NP_004245.2:n.886-51C=
NM_001184732.2:c.886-51C=	NP_001171661.1:n.886-51C=
NM_001184733.2:c.613-51C=	NP_001171662.1:n.613-51C=
NM_001184736.2:c.517-51C=	NP_001171665.1:n.517-51C=