Canonical Allele Identifier: CA1272532

Gene: XPR1

Linked Data

• dbSNP Id: rs752429980
• ExAC: 1:180772629 G / A
• gnomAD v2: 1-180772629-G-A
• gnomAD v3: 1-180803493-G-A
• gnomAD v4: 1-180803493-G-A
• MyVariant Identifiers: chr1:g.180772629G>A (hg19) ; chr1:g.180803493G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803493G>A , CM000663.2:g.180803493G>A	GRCh38
NC_000001.10:g.180772629G>A , CM000663.1:g.180772629G>A	GRCh37
NC_000001.9:g.179039252G>A	NCBI36
NG_050964.1:g.176484G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367590.9:c.329G>A MANE Select	ENSP00000356562.4:p.Arg110His
ENST00000367589.3:c.329G>A	ENSP00000356561.3:p.Arg110His
ENST00000367590.8:c.329G>A	ENSP00000356562.4:p.Arg110His
NM_001135669.1:c.329G>A	NP_001129141.1:p.Arg110His
NM_004736.3:c.329G>A	NP_004727.2:p.Arg110His
NM_001328662.1:c.329G>A	NP_001315591.1:p.Arg110His
NR_137330.1:n.521G>A
NM_001135669.2:c.329G>A	NP_001129141.1:p.Arg110His
NM_001328662.2:c.329G>A	NP_001315591.1:p.Arg110His
NM_004736.4:c.329G>A MANE Select	NP_004727.2:p.Arg110His
NR_137330.2:n.509G>A