Canonical Allele Identifier: CA1210833055
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803471G= , CM000663.2:g.180803471G= GRCh38
NC_000001.10:g.180772607G= , CM000663.1:g.180772607G= GRCh37
NC_000001.9:g.179039230G= NCBI36
NG_050964.1:g.176462G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.307G= MANE Select ENSP00000356562.4:p.Gly103=
ENST00000367589.3:c.307G= ENSP00000356561.3:p.Gly103=
ENST00000367590.8:c.307G= ENSP00000356562.4:p.Gly103=
NM_001135669.1:c.307G= NP_001129141.1:p.Gly103=
NM_004736.3:c.307G= NP_004727.2:p.Gly103=
NM_001328662.1:c.307G= NP_001315591.1:p.Gly103=
NR_137330.1:n.499G=
NM_001135669.2:c.307G= NP_001129141.1:p.Gly103=
NM_001328662.2:c.307G= NP_001315591.1:p.Gly103=
NM_004736.4:c.307G= MANE Select NP_004727.2:p.Gly103=
NR_137330.2:n.487G=