Canonical Allele Identifier: CA343842972
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803430A>G , CM000663.2:g.180803430A>G GRCh38
NC_000001.10:g.180772566A>G , CM000663.1:g.180772566A>G GRCh37
NC_000001.9:g.179039189A>G NCBI36
NG_050964.1:g.176421A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.266A>G MANE Select ENSP00000356562.4:p.Asn89Ser
ENST00000367589.3:c.266A>G ENSP00000356561.3:p.Asn89Ser
ENST00000367590.8:c.266A>G ENSP00000356562.4:p.Asn89Ser
NM_001135669.1:c.266A>G NP_001129141.1:p.Asn89Ser
NM_004736.3:c.266A>G NP_004727.2:p.Asn89Ser
NM_001328662.1:c.266A>G NP_001315591.1:p.Asn89Ser
NR_137330.1:n.458A>G
NM_001135669.2:c.266A>G NP_001129141.1:p.Asn89Ser
NM_001328662.2:c.266A>G NP_001315591.1:p.Asn89Ser
NM_004736.4:c.266A>G MANE Select NP_004727.2:p.Asn89Ser
NR_137330.2:n.446A>G