Canonical Allele Identifier: CA1210833108
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803500G= , CM000663.2:g.180803500G= GRCh38
NC_000001.10:g.180772636G= , CM000663.1:g.180772636G= GRCh37
NC_000001.9:g.179039259G= NCBI36
NG_050964.1:g.176491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.336G= MANE Select ENSP00000356562.4:p.Lys112=
ENST00000367589.3:c.336G= ENSP00000356561.3:p.Lys112=
ENST00000367590.8:c.336G= ENSP00000356562.4:p.Lys112=
NM_001135669.1:c.336G= NP_001129141.1:p.Lys112=
NM_004736.3:c.336G= NP_004727.2:p.Lys112=
NM_001328662.1:c.336G= NP_001315591.1:p.Lys112=
NR_137330.1:n.528G=
NM_001135669.2:c.336G= NP_001129141.1:p.Lys112=
NM_001328662.2:c.336G= NP_001315591.1:p.Lys112=
NM_004736.4:c.336G= MANE Select NP_004727.2:p.Lys112=
NR_137330.2:n.516G=