Canonical Allele Identifier: CA1978013250

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996106A= , CM000673.2:g.62996106A=	GRCh38
NC_000011.9:g.62763578A= , CM000673.1:g.62763578A=	GRCh37
NC_000011.8:g.62520154A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.808T= MANE Select	ENSP00000337335.2:p.Ser270=
ENST00000311438.12:c.808T=	ENSP00000311463.8:p.Ser270=
ENST00000336232.6:c.808T=	ENSP00000337335.2:p.Ser270=
ENST00000430500.6:c.808T=	ENSP00000398548.2:p.Ser270=
ENST00000535878.5:c.439T=	ENSP00000443368.1:p.Ser147=
ENST00000539841.1:n.626T=
ENST00000542795.5:n.529T=
ENST00000542904.1:n.648T=
ENST00000545207.5:c.535T=	ENSP00000441658.1:p.Ser179=
NM_001184732.1:c.808T=	NP_001171661.1:p.Ser270=
NM_001184733.1:c.535T=	NP_001171662.1:p.Ser179=
NM_001184736.1:c.439T=	NP_001171665.1:p.Ser147=
NM_004254.3:c.808T=	NP_004245.2:p.Ser270=
XM_011545364.1:c.439T=	XP_011543666.1:p.Ser147=
NM_004254.4:c.808T= MANE Select	NP_004245.2:p.Ser270=
NM_001184732.2:c.808T=	NP_001171661.1:p.Ser270=
NM_001184733.2:c.535T=	NP_001171662.1:p.Ser179=
NM_001184736.2:c.439T=	NP_001171665.1:p.Ser147=