Canonical Allele Identifier: CA1978013277

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996135A= , CM000673.2:g.62996135A=	GRCh38
NC_000011.9:g.62763607A= , CM000673.1:g.62763607A=	GRCh37
NC_000011.8:g.62520183A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004254.4:c.779T= MANE Select	NP_004245.2:p.Ile260=
ENST00000336232.7:c.779T= MANE Select	ENSP00000337335.2:p.Ile260=
NM_001184732.1:c.779T=	NP_001171661.1:p.Ile260=
NM_001184732.2:c.779T=	NP_001171661.1:p.Ile260=
NM_001184733.1:c.506T=	NP_001171662.1:p.Ile169=
NM_001184733.2:c.506T=	NP_001171662.1:p.Ile169=
NM_001184736.1:c.410T=	NP_001171665.1:p.Ile137=
NM_001184736.2:c.410T=	NP_001171665.1:p.Ile137=
NM_004254.3:c.779T=	NP_004245.2:p.Ile260=
ENST00000311438.12:c.779T=	ENSP00000311463.8:p.Ile260=
ENST00000336232.6:c.779T=	ENSP00000337335.2:p.Ile260=
ENST00000430500.6:c.779T=	ENSP00000398548.2:p.Ile260=
ENST00000535878.5:c.410T=	ENSP00000443368.1:p.Ile137=
ENST00000539841.1:n.597T=
ENST00000542795.5:n.500T=
ENST00000542904.1:n.619T=
ENST00000545207.5:c.506T=	ENSP00000441658.1:p.Ile169=
XM_011545364.1:c.410T=	XP_011543666.1:p.Ile137=