Canonical Allele Identifier: CA380982450
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62996029C>G , CM000673.2:g.62996029C>G GRCh38
NC_000011.9:g.62763501C>G , CM000673.1:g.62763501C>G GRCh37
NC_000011.8:g.62520077C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336232.7:c.885G>C MANE Select ENSP00000337335.2:p.Glu295Asp
ENST00000311438.12:c.885G>C ENSP00000311463.8:p.Glu295Asp
ENST00000336232.6:c.885G>C ENSP00000337335.2:p.Glu295Asp
ENST00000430500.6:c.885G>C ENSP00000398548.2:p.Glu295Asp
ENST00000535878.5:c.516G>C ENSP00000443368.1:p.Glu172Asp
ENST00000539841.1:n.703G>C
ENST00000545207.5:c.612G>C ENSP00000441658.1:p.Glu204Asp
NM_001184732.1:c.885G>C NP_001171661.1:p.Glu295Asp
NM_001184733.1:c.612G>C NP_001171662.1:p.Glu204Asp
NM_001184736.1:c.516G>C NP_001171665.1:p.Glu172Asp
NM_004254.3:c.885G>C NP_004245.2:p.Glu295Asp
XM_011545364.1:c.516G>C XP_011543666.1:p.Glu172Asp
NM_004254.4:c.885G>C MANE Select NP_004245.2:p.Glu295Asp
NM_001184732.2:c.885G>C NP_001171661.1:p.Glu295Asp
NM_001184733.2:c.612G>C NP_001171662.1:p.Glu204Asp
NM_001184736.2:c.516G>C NP_001171665.1:p.Glu172Asp