Canonical Allele Identifier: CA1210832924

Gene: XPR1

Linked Data

• dbSNP Id: rs1649863571
• gnomAD v4: 1-180803334-CAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803337_180803339del , CM000663.2:g.180803337_180803339del	GRCh38
NC_000001.10:g.180772473_180772475del , CM000663.1:g.180772473_180772475del	GRCh37
NC_000001.9:g.179039096_179039098del	NCBI36
NG_050964.1:g.176328_176330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.224-51_224-49del MANE Select	ENSP00000356562.4:n.224-51_224-49del
ENST00000367589.3:c.224-51_224-49del	ENSP00000356561.3:n.224-51_224-49del
ENST00000367590.8:c.224-51_224-49del	ENSP00000356562.4:n.224-51_224-49del
NM_001135669.1:c.224-51_224-49del	NP_001129141.1:n.224-51_224-49del
NM_004736.3:c.224-51_224-49del	NP_004727.2:n.224-51_224-49del
NM_001328662.1:c.224-51_224-49del	NP_001315591.1:n.224-51_224-49del
NR_137330.1:n.416-51_416-49del
NM_001135669.2:c.224-51_224-49del	NP_001129141.1:n.224-51_224-49del
NM_001328662.2:c.224-51_224-49del	NP_001315591.1:n.224-51_224-49del
NM_004736.4:c.224-51_224-49del MANE Select	NP_004727.2:n.224-51_224-49del
NR_137330.2:n.404-51_404-49del