Canonical Allele Identifier: CA422226205

Gene: XPR1

Linked Data

• MyVariant Identifiers: chr1:g.180772591A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803455A>T , CM000663.2:g.180803455A>T	GRCh38
NC_000001.10:g.180772591A>T , CM000663.1:g.180772591A>T	GRCh37
NC_000001.9:g.179039214A>T	NCBI36
NG_050964.1:g.176446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.291A>T MANE Select	ENSP00000356562.4:p.Ala97=
ENST00000367589.3:c.291A>T	ENSP00000356561.3:p.Ala97=
ENST00000367590.8:c.291A>T	ENSP00000356562.4:p.Ala97=
NM_001135669.1:c.291A>T	NP_001129141.1:p.Ala97=
NM_004736.3:c.291A>T	NP_004727.2:p.Ala97=
NM_001328662.1:c.291A>T	NP_001315591.1:p.Ala97=
NR_137330.1:n.483A>T
NM_001135669.2:c.291A>T	NP_001129141.1:p.Ala97=
NM_001328662.2:c.291A>T	NP_001315591.1:p.Ala97=
NM_004736.4:c.291A>T MANE Select	NP_004727.2:p.Ala97=
NR_137330.2:n.471A>T