Canonical Allele Identifier: CA354870749

Gene: XRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142311632T>G , CM000665.2:g.142311632T>G	GRCh38
NC_000003.11:g.142030474T>G , CM000665.1:g.142030474T>G	GRCh37
NC_000003.10:g.143513164T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001282857.2:c.4964A>C MANE Select	NP_001269786.1:p.Gln1655Pro
ENST00000392981.7:c.4964A>C MANE Select	ENSP00000376707.2:p.Gln1655Pro
NM_001282857.1:c.4964A>C	NP_001269786.1:p.Gln1655Pro
NM_019001.4:c.5000A>C	NP_061874.3:p.Gln1667Pro
NM_019001.5:c.5000A>C	NP_061874.3:p.Gln1667Pro
ENST00000264951.8:c.5000A>C	ENSP00000264951.4:p.Gln1667Pro
ENST00000392981.6:c.4964A>C	ENSP00000376707.2:p.Gln1655Pro
ENST00000498077.6:c.3360A>C
XM_011512919.1:c.5003A>C	XP_011511221.1:p.Gln1668Pro
XM_011512919.2:c.5003A>C	XP_011511221.1:p.Gln1668Pro
XM_011512920.1:c.4889A>C	XP_011511222.1:p.Gln1630Pro
XM_011512920.2:c.4889A>C	XP_011511222.1:p.Gln1630Pro
XM_011512921.1:c.4586A>C	XP_011511223.1:p.Gln1529Pro
XM_011512922.1:c.4373A>C	XP_011511224.1:p.Gln1458Pro
XM_011512922.2:c.4373A>C	XP_011511224.1:p.Gln1458Pro
XM_017006640.1:c.4961A>C	XP_016862129.1:p.Gln1654Pro
XM_017006641.1:c.4850A>C	XP_016862130.1:p.Gln1617Pro
XR_001740178.1:n.5104A>C