Canonical Allele Identifier: CA1210832898
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803307A= , CM000663.2:g.180803307A= GRCh38
NC_000001.10:g.180772443A= , CM000663.1:g.180772443A= GRCh37
NC_000001.9:g.179039066A= NCBI36
NG_050964.1:g.176298A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.224-81A= MANE Select ENSP00000356562.4:n.224-81A=
ENST00000367589.3:c.224-81A= ENSP00000356561.3:n.224-81A=
ENST00000367590.8:c.224-81A= ENSP00000356562.4:n.224-81A=
NM_001135669.1:c.224-81A= NP_001129141.1:n.224-81A=
NM_004736.3:c.224-81A= NP_004727.2:n.224-81A=
NM_001328662.1:c.224-81A= NP_001315591.1:n.224-81A=
NR_137330.1:n.416-81A=
NM_001135669.2:c.224-81A= NP_001129141.1:n.224-81A=
NM_001328662.2:c.224-81A= NP_001315591.1:n.224-81A=
NM_004736.4:c.224-81A= MANE Select NP_004727.2:n.224-81A=
NR_137330.2:n.404-81A=