Canonical Allele Identifier: CA1142027123
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803398A= , CM000663.2:g.180803398A= GRCh38
NC_000001.10:g.180772534A= , CM000663.1:g.180772534A= GRCh37
NC_000001.9:g.179039157A= NCBI36
NG_050964.1:g.176389A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.234A= MANE Select ENSP00000356562.4:p.Ala78=
ENST00000367589.3:c.234A= ENSP00000356561.3:p.Ala78=
ENST00000367590.8:c.234A= ENSP00000356562.4:p.Ala78=
NM_001135669.1:c.234A= NP_001129141.1:p.Ala78=
NM_004736.3:c.234A= NP_004727.2:p.Ala78=
NM_001328662.1:c.234A= NP_001315591.1:p.Ala78=
NR_137330.1:n.426A=
NM_001135669.2:c.234A= NP_001129141.1:p.Ala78=
NM_001328662.2:c.234A= NP_001315591.1:p.Ala78=
NM_004736.4:c.234A= MANE Select NP_004727.2:p.Ala78=
NR_137330.2:n.414A=