Canonical Allele Identifier: CA354794820
Community Standard Title: NM_001282857.2(XRN1):c.2670C>G (p.Ser890Arg)
Gene: XRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142380127G>C , CM000665.2:g.142380127G>C GRCh38
NC_000003.11:g.142098969G>C , CM000665.1:g.142098969G>C GRCh37
NC_000003.10:g.143581659G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001282857.2:c.2670C>G MANE Select NP_001269786.1:p.Ser890Arg
ENST00000392981.7:c.2670C>G MANE Select ENSP00000376707.2:p.Ser890Arg
NM_001282857.1:c.2670C>G NP_001269786.1:p.Ser890Arg
NM_019001.4:c.2670C>G NP_061874.3:p.Ser890Arg
NM_019001.5:c.2670C>G NP_061874.3:p.Ser890Arg
ENST00000264951.8:c.2670C>G ENSP00000264951.4:p.Ser890Arg
ENST00000392981.6:c.2670C>G ENSP00000376707.2:p.Ser890Arg
ENST00000472697.5:n.2261C>G
ENST00000498077.6:c.1066C>G
XM_006713673.2:c.2670C>G XP_006713736.1:p.Ser890Arg
XM_011512919.1:c.2670C>G XP_011511221.1:p.Ser890Arg
XM_011512919.2:c.2670C>G XP_011511221.1:p.Ser890Arg
XM_011512920.1:c.2670C>G XP_011511222.1:p.Ser890Arg
XM_011512920.2:c.2670C>G XP_011511222.1:p.Ser890Arg
XM_011512921.1:c.2253C>G XP_011511223.1:p.Ser751Arg
XM_011512922.1:c.2040C>G XP_011511224.1:p.Ser680Arg
XM_011512922.2:c.2040C>G XP_011511224.1:p.Ser680Arg
XM_011512923.1:c.2670C>G XP_011511225.1:p.Ser890Arg
XM_017006640.1:c.2670C>G XP_016862129.1:p.Ser890Arg
XM_017006641.1:c.2670C>G XP_016862130.1:p.Ser890Arg
XM_017006642.1:c.2670C>G XP_016862131.1:p.Ser890Arg
XR_001740178.1:n.2788C>G