Canonical Allele Identifier: CA1978013275

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996134T= , CM000673.2:g.62996134T=	GRCh38
NC_000011.9:g.62763606T= , CM000673.1:g.62763606T=	GRCh37
NC_000011.8:g.62520182T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.780A= MANE Select	ENSP00000337335.2:p.Ile260=
ENST00000311438.12:c.780A=	ENSP00000311463.8:p.Ile260=
ENST00000336232.6:c.780A=	ENSP00000337335.2:p.Ile260=
ENST00000430500.6:c.780A=	ENSP00000398548.2:p.Ile260=
ENST00000535878.5:c.411A=	ENSP00000443368.1:p.Ile137=
ENST00000539841.1:n.598A=
ENST00000542795.5:n.501A=
ENST00000542904.1:n.620A=
ENST00000545207.5:c.507A=	ENSP00000441658.1:p.Ile169=
NM_001184732.1:c.780A=	NP_001171661.1:p.Ile260=
NM_001184733.1:c.507A=	NP_001171662.1:p.Ile169=
NM_001184736.1:c.411A=	NP_001171665.1:p.Ile137=
NM_004254.3:c.780A=	NP_004245.2:p.Ile260=
XM_011545364.1:c.411A=	XP_011543666.1:p.Ile137=
NM_004254.4:c.780A= MANE Select	NP_004245.2:p.Ile260=
NM_001184732.2:c.780A=	NP_001171661.1:p.Ile260=
NM_001184733.2:c.507A=	NP_001171662.1:p.Ile169=
NM_001184736.2:c.411A=	NP_001171665.1:p.Ile137=