Canonical Allele Identifier: CA1978015815

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998940C= , CM000673.2:g.62998940C=	GRCh38
NC_000011.9:g.62766412C= , CM000673.1:g.62766412C=	GRCh37
NC_000011.8:g.62522988C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.742G= MANE Select	ENSP00000337335.2:p.Val248=
ENST00000311438.12:c.742G=	ENSP00000311463.8:p.Val248=
ENST00000336232.6:c.742G=	ENSP00000337335.2:p.Val248=
ENST00000430500.6:c.742G=	ENSP00000398548.2:p.Val248=
ENST00000535878.5:c.373G=	ENSP00000443368.1:p.Val125=
ENST00000539841.1:n.560G=
ENST00000542795.5:n.463G=
ENST00000542904.1:n.582G=
ENST00000545207.5:c.469G=	ENSP00000441658.1:p.Val157=
NM_001184732.1:c.742G=	NP_001171661.1:p.Val248=
NM_001184733.1:c.469G=	NP_001171662.1:p.Val157=
NM_001184736.1:c.373G=	NP_001171665.1:p.Val125=
NM_004254.3:c.742G=	NP_004245.2:p.Val248=
XM_011545364.1:c.373G=	XP_011543666.1:p.Val125=
NM_004254.4:c.742G= MANE Select	NP_004245.2:p.Val248=
NM_001184732.2:c.742G=	NP_001171661.1:p.Val248=
NM_001184733.2:c.469G=	NP_001171662.1:p.Val157=
NM_001184736.2:c.373G=	NP_001171665.1:p.Val125=