Canonical Allele Identifier: CA2648444

Gene: XRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142403711A>G , CM000665.2:g.142403711A>G	GRCh38
NC_000003.11:g.142122553A>G , CM000665.1:g.142122553A>G	GRCh37
NC_000003.10:g.143605243A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392981.7:c.2066T>C MANE Select	ENSP00000376707.2:p.Met689Thr
ENST00000264951.8:c.2066T>C	ENSP00000264951.4:p.Met689Thr
ENST00000392981.6:c.2066T>C	ENSP00000376707.2:p.Met689Thr
ENST00000472697.5:n.1657T>C
ENST00000498077.6:c.462T>C
NM_001282857.1:c.2066T>C	NP_001269786.1:p.Met689Thr
NM_019001.4:c.2066T>C	NP_061874.3:p.Met689Thr
XM_006713673.2:c.2066T>C	XP_006713736.1:p.Met689Thr
XM_011512919.1:c.2066T>C	XP_011511221.1:p.Met689Thr
XM_011512920.1:c.2066T>C	XP_011511222.1:p.Met689Thr
XM_011512921.1:c.1649T>C	XP_011511223.1:p.Met550Thr
XM_011512922.1:c.1436T>C	XP_011511224.1:p.Met479Thr
XM_011512923.1:c.2066T>C	XP_011511225.1:p.Met689Thr
XM_011512919.2:c.2066T>C	XP_011511221.1:p.Met689Thr
XM_011512920.2:c.2066T>C	XP_011511222.1:p.Met689Thr
XM_011512922.2:c.1436T>C	XP_011511224.1:p.Met479Thr
XM_017006640.1:c.2066T>C	XP_016862129.1:p.Met689Thr
XM_017006641.1:c.2066T>C	XP_016862130.1:p.Met689Thr
XM_017006642.1:c.2066T>C	XP_016862131.1:p.Met689Thr
XR_001740178.1:n.2184T>C
NM_001282857.2:c.2066T>C MANE Select	NP_001269786.1:p.Met689Thr
NM_019001.5:c.2066T>C	NP_061874.3:p.Met689Thr