Canonical Allele Identifier: CA2794458576
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793057_7793058dup , CM000674.2:g.7793057_7793058dup GRCh38
NC_000012.11:g.7945653_7945654dup , CM000674.1:g.7945653_7945654dup GRCh37
NC_000012.10:g.7836920_7836921dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.259_260dup MANE Select ENSP00000229307.4:p.Glu88ArgfsTer?
ENST00000229307.8:c.259_260dup ENSP00000229307.4:p.Glu88ArgfsTer?
ENST00000526286.1:c.259_260dup ENSP00000435288.1:p.Glu88ArgfsTer?
ENST00000526434.2:n.403_404dup
ENST00000541267.5:c.187_188dup ENSP00000444434.1:p.Glu64ArgfsTer?
NM_001297698.1:c.259_260dup NP_001284627.1:p.Glu88ArgfsTer?
NM_024865.3:c.259_260dup NP_079141.2:p.Glu88ArgfsTer?
XM_011520850.1:c.259_260dup XP_011519152.1:p.Glu88ArgfsTer?
XM_011520851.1:c.187_188dup XP_011519153.1:p.Glu64ArgfsTer?
XM_011520852.1:c.-114_-113dup XP_011519154.1:n.-114_-113dup
NM_024865.4:c.259_260dup MANE Select NP_079141.2:p.Glu88ArgfsTer?
NM_001297698.2:c.259_260dup NP_001284627.1:p.Glu88ArgfsTer?