Canonical Allele Identifier: CA354821677

Gene: XRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142376570C>T , CM000665.2:g.142376570C>T	GRCh38
NC_000003.11:g.142095412C>T , CM000665.1:g.142095412C>T	GRCh37
NC_000003.10:g.143578102C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392981.7:c.2740G>A MANE Select	ENSP00000376707.2:p.Gly914Arg
ENST00000264951.8:c.2740G>A	ENSP00000264951.4:p.Gly914Arg
ENST00000392981.6:c.2740G>A	ENSP00000376707.2:p.Gly914Arg
ENST00000472697.5:n.2331G>A
ENST00000498077.6:c.1136G>A
NM_001282857.1:c.2740G>A	NP_001269786.1:p.Gly914Arg
NM_019001.4:c.2740G>A	NP_061874.3:p.Gly914Arg
XM_006713673.2:c.*52G>A	XP_006713736.1:n.*52G>A
XM_011512919.1:c.2740G>A	XP_011511221.1:p.Gly914Arg
XM_011512920.1:c.2740G>A	XP_011511222.1:p.Gly914Arg
XM_011512921.1:c.2323G>A	XP_011511223.1:p.Gly775Arg
XM_011512922.1:c.2110G>A	XP_011511224.1:p.Gly704Arg
XM_011512923.1:c.2740G>A	XP_011511225.1:p.Gly914Arg
XM_011512919.2:c.2740G>A	XP_011511221.1:p.Gly914Arg
XM_011512920.2:c.2740G>A	XP_011511222.1:p.Gly914Arg
XM_011512922.2:c.2110G>A	XP_011511224.1:p.Gly704Arg
XM_017006640.1:c.2740G>A	XP_016862129.1:p.Gly914Arg
XM_017006641.1:c.2740G>A	XP_016862130.1:p.Gly914Arg
XM_017006642.1:c.2740G>A	XP_016862131.1:p.Gly914Arg
XR_001740178.1:n.2858G>A
NM_001282857.2:c.2740G>A MANE Select	NP_001269786.1:p.Gly914Arg
NM_019001.5:c.2740G>A	NP_061874.3:p.Gly914Arg