Canonical Allele Identifier: CA422226223
Gene: XPR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.180772621G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803485G>A , CM000663.2:g.180803485G>A GRCh38
NC_000001.10:g.180772621G>A , CM000663.1:g.180772621G>A GRCh37
NC_000001.9:g.179039244G>A NCBI36
NG_050964.1:g.176476G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.321G>A MANE Select ENSP00000356562.4:p.Leu107=
ENST00000367589.3:c.321G>A ENSP00000356561.3:p.Leu107=
ENST00000367590.8:c.321G>A ENSP00000356562.4:p.Leu107=
NM_001135669.1:c.321G>A NP_001129141.1:p.Leu107=
NM_004736.3:c.321G>A NP_004727.2:p.Leu107=
NM_001328662.1:c.321G>A NP_001315591.1:p.Leu107=
NR_137330.1:n.513G>A
NM_001135669.2:c.321G>A NP_001129141.1:p.Leu107=
NM_001328662.2:c.321G>A NP_001315591.1:p.Leu107=
NM_004736.4:c.321G>A MANE Select NP_004727.2:p.Leu107=
NR_137330.2:n.501G>A