Canonical Allele Identifier: CA1210835619
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180806529T= , CM000663.2:g.180806529T= GRCh38
NC_000001.10:g.180775665T= , CM000663.1:g.180775665T= GRCh37
NC_000001.9:g.179042288T= NCBI36
NG_050964.1:g.179520T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.653T= MANE Select ENSP00000356562.4:p.Leu218=
ENST00000367589.3:c.653T= ENSP00000356561.3:p.Leu218=
ENST00000367590.8:c.653T= ENSP00000356562.4:p.Leu218=
NM_001135669.1:c.653T= NP_001129141.1:p.Leu218=
NM_004736.3:c.653T= NP_004727.2:p.Leu218=
NM_001328662.1:c.653T= NP_001315591.1:p.Leu218=
NR_137330.1:n.845T=
NM_001135669.2:c.653T= NP_001129141.1:p.Leu218=
NM_001328662.2:c.653T= NP_001315591.1:p.Leu218=
NM_004736.4:c.653T= MANE Select NP_004727.2:p.Leu218=
NR_137330.2:n.833T=