Canonical Allele Identifier: CA422226211

Gene: XPR1

Linked Data

• MyVariant Identifiers: chr1:g.180772606T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803470T>A , CM000663.2:g.180803470T>A	GRCh38
NC_000001.10:g.180772606T>A , CM000663.1:g.180772606T>A	GRCh37
NC_000001.9:g.179039229T>A	NCBI36
NG_050964.1:g.176461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.306T>A MANE Select	ENSP00000356562.4:p.Thr102=
ENST00000367589.3:c.306T>A	ENSP00000356561.3:p.Thr102=
ENST00000367590.8:c.306T>A	ENSP00000356562.4:p.Thr102=
NM_001135669.1:c.306T>A	NP_001129141.1:p.Thr102=
NM_004736.3:c.306T>A	NP_004727.2:p.Thr102=
NM_001328662.1:c.306T>A	NP_001315591.1:p.Thr102=
NR_137330.1:n.498T>A
NM_001135669.2:c.306T>A	NP_001129141.1:p.Thr102=
NM_001328662.2:c.306T>A	NP_001315591.1:p.Thr102=
NM_004736.4:c.306T>A MANE Select	NP_004727.2:p.Thr102=
NR_137330.2:n.486T>A