Canonical Allele Identifier: CA1978016057

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999080C= , CM000673.2:g.62999080C=	GRCh38
NC_000011.9:g.62766552C= , CM000673.1:g.62766552C=	GRCh37
NC_000011.8:g.62523128C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.602G= MANE Select	ENSP00000337335.2:p.Trp201=
ENST00000311438.12:c.602G=	ENSP00000311463.8:p.Trp201=
ENST00000336232.6:c.602G=	ENSP00000337335.2:p.Trp201=
ENST00000430500.6:c.602G=	ENSP00000398548.2:p.Trp201=
ENST00000535878.5:c.233G=	ENSP00000443368.1:p.Trp78=
ENST00000539841.1:n.420G=
ENST00000542795.5:n.323G=
ENST00000542904.1:n.442G=
ENST00000545207.5:c.329G=	ENSP00000441658.1:p.Trp110=
NM_001184732.1:c.602G=	NP_001171661.1:p.Trp201=
NM_001184733.1:c.329G=	NP_001171662.1:p.Trp110=
NM_001184736.1:c.233G=	NP_001171665.1:p.Trp78=
NM_004254.3:c.602G=	NP_004245.2:p.Trp201=
XM_011545364.1:c.233G=	XP_011543666.1:p.Trp78=
NM_004254.4:c.602G= MANE Select	NP_004245.2:p.Trp201=
NM_001184732.2:c.602G=	NP_001171661.1:p.Trp201=
NM_001184733.2:c.329G=	NP_001171662.1:p.Trp110=
NM_001184736.2:c.233G=	NP_001171665.1:p.Trp78=