Canonical Allele Identifier: CA2649367367
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803323A>C , CM000663.2:g.180803323A>C GRCh38
NC_000001.10:g.180772459A>C , CM000663.1:g.180772459A>C GRCh37
NC_000001.9:g.179039082A>C NCBI36
NG_050964.1:g.176314A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.224-65A>C MANE Select ENSP00000356562.4:n.224-65A>C
ENST00000367589.3:c.224-65A>C ENSP00000356561.3:n.224-65A>C
ENST00000367590.8:c.224-65A>C ENSP00000356562.4:n.224-65A>C
NM_001135669.1:c.224-65A>C NP_001129141.1:n.224-65A>C
NM_004736.3:c.224-65A>C NP_004727.2:n.224-65A>C
NM_001328662.1:c.224-65A>C NP_001315591.1:n.224-65A>C
NR_137330.1:n.416-65A>C
NM_001135669.2:c.224-65A>C NP_001129141.1:n.224-65A>C
NM_001328662.2:c.224-65A>C NP_001315591.1:n.224-65A>C
NM_004736.4:c.224-65A>C MANE Select NP_004727.2:n.224-65A>C
NR_137330.2:n.404-65A>C