Canonical Allele Identifier: CA1272516
Gene: XPR1 HGNC NCBI

Linked Data

dbSNP Id: rs758536049

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803403C>G , CM000663.2:g.180803403C>G GRCh38
NC_000001.10:g.180772539C>G , CM000663.1:g.180772539C>G GRCh37
NC_000001.9:g.179039162C>G NCBI36
NG_050964.1:g.176394C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.239C>G MANE Select ENSP00000356562.4:p.Ala80Gly
ENST00000367589.3:c.239C>G ENSP00000356561.3:p.Ala80Gly
ENST00000367590.8:c.239C>G ENSP00000356562.4:p.Ala80Gly
NM_001135669.1:c.239C>G NP_001129141.1:p.Ala80Gly
NM_004736.3:c.239C>G NP_004727.2:p.Ala80Gly
NM_001328662.1:c.239C>G NP_001315591.1:p.Ala80Gly
NR_137330.1:n.431C>G
NM_001135669.2:c.239C>G NP_001129141.1:p.Ala80Gly
NM_001328662.2:c.239C>G NP_001315591.1:p.Ala80Gly
NM_004736.4:c.239C>G MANE Select NP_004727.2:p.Ala80Gly
NR_137330.2:n.419C>G