Canonical Allele Identifier: CA645575933

Gene: SLC22A8

Linked Data - Expert Curation

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996085_62996086delinsAA , CM000673.2:g.62996085_62996086delinsAA	GRCh38
NC_000011.9:g.62763557_62763558delinsAA , CM000673.1:g.62763557_62763558delinsAA	GRCh37
NC_000011.8:g.62520133_62520134delinsAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.828_829delinsTT MANE Select	ENSP00000337335.2:p.Arg277Trp
ENST00000311438.12:c.828_829delinsTT	ENSP00000311463.8:p.Arg277Trp
ENST00000336232.6:c.828_829delinsTT	ENSP00000337335.2:p.Arg277Trp
ENST00000430500.6:c.828_829delinsTT	ENSP00000398548.2:p.Arg277Trp
ENST00000535878.5:c.459_460delinsTT	ENSP00000443368.1:p.Arg154Trp
ENST00000539841.1:n.646_647delinsTT
ENST00000545207.5:c.555_556delinsTT	ENSP00000441658.1:p.Arg186Trp
NM_001184732.1:c.828_829delinsTT	NP_001171661.1:p.Arg277Trp
NM_001184733.1:c.555_556delinsTT	NP_001171662.1:p.Arg186Trp
NM_001184736.1:c.459_460delinsTT	NP_001171665.1:p.Arg154Trp
NM_004254.3:c.828_829delinsTT	NP_004245.2:p.Arg277Trp
XM_011545364.1:c.459_460delinsTT	XP_011543666.1:p.Arg154Trp
NM_004254.4:c.828_829delinsTT MANE Select	NP_004245.2:p.Arg277Trp
NM_001184732.2:c.828_829delinsTT	NP_001171661.1:p.Arg277Trp
NM_001184733.2:c.555_556delinsTT	NP_001171662.1:p.Arg186Trp
NM_001184736.2:c.459_460delinsTT	NP_001171665.1:p.Arg154Trp