Canonical Allele Identifier: CA343843020
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803453G>A , CM000663.2:g.180803453G>A GRCh38
NC_000001.10:g.180772589G>A , CM000663.1:g.180772589G>A GRCh37
NC_000001.9:g.179039212G>A NCBI36
NG_050964.1:g.176444G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.289G>A MANE Select ENSP00000356562.4:p.Ala97Thr
ENST00000367589.3:c.289G>A ENSP00000356561.3:p.Ala97Thr
ENST00000367590.8:c.289G>A ENSP00000356562.4:p.Ala97Thr
NM_001135669.1:c.289G>A NP_001129141.1:p.Ala97Thr
NM_004736.3:c.289G>A NP_004727.2:p.Ala97Thr
NM_001328662.1:c.289G>A NP_001315591.1:p.Ala97Thr
NR_137330.1:n.481G>A
NM_001135669.2:c.289G>A NP_001129141.1:p.Ala97Thr
NM_001328662.2:c.289G>A NP_001315591.1:p.Ala97Thr
NM_004736.4:c.289G>A MANE Select NP_004727.2:p.Ala97Thr
NR_137330.2:n.469G>A