Canonical Allele Identifier: CA343843319
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803585A>T , CM000663.2:g.180803585A>T GRCh38
NC_000001.10:g.180772721A>T , CM000663.1:g.180772721A>T GRCh37
NC_000001.9:g.179039344A>T NCBI36
NG_050964.1:g.176576A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.421A>T MANE Select ENSP00000356562.4:p.Ser141Cys
ENST00000367589.3:c.421A>T ENSP00000356561.3:p.Ser141Cys
ENST00000367590.8:c.421A>T ENSP00000356562.4:p.Ser141Cys
NM_001135669.1:c.421A>T NP_001129141.1:p.Ser141Cys
NM_004736.3:c.421A>T NP_004727.2:p.Ser141Cys
NM_001328662.1:c.421A>T NP_001315591.1:p.Ser141Cys
NR_137330.1:n.613A>T
NM_001135669.2:c.421A>T NP_001129141.1:p.Ser141Cys
NM_001328662.2:c.421A>T NP_001315591.1:p.Ser141Cys
NM_004736.4:c.421A>T MANE Select NP_004727.2:p.Ser141Cys
NR_137330.2:n.601A>T