Canonical Allele Identifier: CA1210833247

Gene: XPR1

Linked Data

• dbSNP Id: rs1571853217
• gnomAD v4: 1-180803667-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803667T>C , CM000663.2:g.180803667T>C	GRCh38
NC_000001.10:g.180772803T>C , CM000663.1:g.180772803T>C	GRCh37
NC_000001.9:g.179039426T>C	NCBI36
NG_050964.1:g.176658T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.447+56T>C MANE Select	ENSP00000356562.4:n.447+56T>C
ENST00000367589.3:c.447+56T>C	ENSP00000356561.3:n.447+56T>C
ENST00000367590.8:c.447+56T>C	ENSP00000356562.4:n.447+56T>C
NM_001135669.1:c.447+56T>C	NP_001129141.1:n.447+56T>C
NM_004736.3:c.447+56T>C	NP_004727.2:n.447+56T>C
NM_001328662.1:c.447+56T>C	NP_001315591.1:n.447+56T>C
NR_137330.1:n.639+56T>C
NM_001135669.2:c.447+56T>C	NP_001129141.1:n.447+56T>C
NM_001328662.2:c.447+56T>C	NP_001315591.1:n.447+56T>C
NM_004736.4:c.447+56T>C MANE Select	NP_004727.2:n.447+56T>C
NR_137330.2:n.627+56T>C