Canonical Allele Identifier: CA1210832943

Gene: XPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803359_180803360delinsAT , CM000663.2:g.180803359_180803360delinsAT	GRCh38
NC_000001.10:g.180772495_180772496delinsAT , CM000663.1:g.180772495_180772496delinsAT	GRCh37
NC_000001.9:g.179039118_179039119delinsAT	NCBI36
NG_050964.1:g.176350_176351delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.224-29_224-28delinsAT MANE Select	ENSP00000356562.4:n.224-29_224-28delinsAT
ENST00000367589.3:c.224-29_224-28delinsAT	ENSP00000356561.3:n.224-29_224-28delinsAT
ENST00000367590.8:c.224-29_224-28delinsAT	ENSP00000356562.4:n.224-29_224-28delinsAT
NM_001135669.1:c.224-29_224-28delinsAT	NP_001129141.1:n.224-29_224-28delinsAT
NM_004736.3:c.224-29_224-28delinsAT	NP_004727.2:n.224-29_224-28delinsAT
NM_001328662.1:c.224-29_224-28delinsAT	NP_001315591.1:n.224-29_224-28delinsAT
NR_137330.1:n.416-29_416-28delinsAT
NM_001135669.2:c.224-29_224-28delinsAT	NP_001129141.1:n.224-29_224-28delinsAT
NM_001328662.2:c.224-29_224-28delinsAT	NP_001315591.1:n.224-29_224-28delinsAT
NM_004736.4:c.224-29_224-28delinsAT MANE Select	NP_004727.2:n.224-29_224-28delinsAT
NR_137330.2:n.404-29_404-28delinsAT