Canonical Allele Identifier: CA1272528

Gene: XPR1

Linked Data

• dbSNP Id: rs150752401
• ExAC: 1:180772618 G / T
• gnomAD v2: 1-180772618-G-T
• gnomAD v3: 1-180803482-G-T
• gnomAD v4: 1-180803482-G-T
• MyVariant Identifiers: chr1:g.180772618G>T (hg19) ; chr1:g.180803482G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803482G>T , CM000663.2:g.180803482G>T	GRCh38
NC_000001.10:g.180772618G>T , CM000663.1:g.180772618G>T	GRCh37
NC_000001.9:g.179039241G>T	NCBI36
NG_050964.1:g.176473G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.318G>T MANE Select	ENSP00000356562.4:p.Thr106=
ENST00000367589.3:c.318G>T	ENSP00000356561.3:p.Thr106=
ENST00000367590.8:c.318G>T	ENSP00000356562.4:p.Thr106=
NM_001135669.1:c.318G>T	NP_001129141.1:p.Thr106=
NM_004736.3:c.318G>T	NP_004727.2:p.Thr106=
NM_001328662.1:c.318G>T	NP_001315591.1:p.Thr106=
NR_137330.1:n.510G>T
NM_001135669.2:c.318G>T	NP_001129141.1:p.Thr106=
NM_001328662.2:c.318G>T	NP_001315591.1:p.Thr106=
NM_004736.4:c.318G>T MANE Select	NP_004727.2:p.Thr106=
NR_137330.2:n.498G>T