Canonical Allele Identifier: CA1210832935

Gene: XPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803343_180803344delinsCT , CM000663.2:g.180803343_180803344delinsCT	GRCh38
NC_000001.10:g.180772479_180772480delinsCT , CM000663.1:g.180772479_180772480delinsCT	GRCh37
NC_000001.9:g.179039102_179039103delinsCT	NCBI36
NG_050964.1:g.176334_176335delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.224-45_224-44delinsCT MANE Select	ENSP00000356562.4:n.224-45_224-44delinsCT
ENST00000367589.3:c.224-45_224-44delinsCT	ENSP00000356561.3:n.224-45_224-44delinsCT
ENST00000367590.8:c.224-45_224-44delinsCT	ENSP00000356562.4:n.224-45_224-44delinsCT
NM_001135669.1:c.224-45_224-44delinsCT	NP_001129141.1:n.224-45_224-44delinsCT
NM_004736.3:c.224-45_224-44delinsCT	NP_004727.2:n.224-45_224-44delinsCT
NM_001328662.1:c.224-45_224-44delinsCT	NP_001315591.1:n.224-45_224-44delinsCT
NR_137330.1:n.416-45_416-44delinsCT
NM_001135669.2:c.224-45_224-44delinsCT	NP_001129141.1:n.224-45_224-44delinsCT
NM_001328662.2:c.224-45_224-44delinsCT	NP_001315591.1:n.224-45_224-44delinsCT
NM_004736.4:c.224-45_224-44delinsCT MANE Select	NP_004727.2:n.224-45_224-44delinsCT
NR_137330.2:n.404-45_404-44delinsCT