Canonical Allele Identifier: CA422226220

Gene: XPR1

Linked Data

• MyVariant Identifiers: chr1:g.180772615T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803479T>G , CM000663.2:g.180803479T>G	GRCh38
NC_000001.10:g.180772615T>G , CM000663.1:g.180772615T>G	GRCh37
NC_000001.9:g.179039238T>G	NCBI36
NG_050964.1:g.176470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.315T>G MANE Select	ENSP00000356562.4:p.Thr105=
ENST00000367589.3:c.315T>G	ENSP00000356561.3:p.Thr105=
ENST00000367590.8:c.315T>G	ENSP00000356562.4:p.Thr105=
NM_001135669.1:c.315T>G	NP_001129141.1:p.Thr105=
NM_004736.3:c.315T>G	NP_004727.2:p.Thr105=
NM_001328662.1:c.315T>G	NP_001315591.1:p.Thr105=
NR_137330.1:n.507T>G
NM_001135669.2:c.315T>G	NP_001129141.1:p.Thr105=
NM_001328662.2:c.315T>G	NP_001315591.1:p.Thr105=
NM_004736.4:c.315T>G MANE Select	NP_004727.2:p.Thr105=
NR_137330.2:n.495T>G