Canonical Allele Identifier: CA343842891
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803393C>G , CM000663.2:g.180803393C>G GRCh38
NC_000001.10:g.180772529C>G , CM000663.1:g.180772529C>G GRCh37
NC_000001.9:g.179039152C>G NCBI36
NG_050964.1:g.176384C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.229C>G MANE Select ENSP00000356562.4:p.Leu77Val
ENST00000367589.3:c.229C>G ENSP00000356561.3:p.Leu77Val
ENST00000367590.8:c.229C>G ENSP00000356562.4:p.Leu77Val
NM_001135669.1:c.229C>G NP_001129141.1:p.Leu77Val
NM_004736.3:c.229C>G NP_004727.2:p.Leu77Val
NM_001328662.1:c.229C>G NP_001315591.1:p.Leu77Val
NR_137330.1:n.421C>G
NM_001135669.2:c.229C>G NP_001129141.1:p.Leu77Val
NM_001328662.2:c.229C>G NP_001315591.1:p.Leu77Val
NM_004736.4:c.229C>G MANE Select NP_004727.2:p.Leu77Val
NR_137330.2:n.409C>G