Canonical Allele Identifier: CA2794458575

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793058_7793059insAAAAAAAAAAA , CM000674.2:g.7793058_7793059insAAAAAAAAAAA	GRCh38
NC_000012.11:g.7945654_7945655insAAAAAAAAAAA , CM000674.1:g.7945654_7945655insAAAAAAAAAAA	GRCh37
NC_000012.10:g.7836921_7836922insAAAAAAAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.260_261insAAAAAAAAAAA MANE Select	ENSP00000229307.4:p.Glu88LysfsTer?
ENST00000229307.8:c.260_261insAAAAAAAAAAA	ENSP00000229307.4:p.Glu88LysfsTer?
ENST00000526286.1:c.260_261insAAAAAAAAAAA	ENSP00000435288.1:p.Glu88LysfsTer?
ENST00000526434.2:n.404_405insAAAAAAAAAAA
ENST00000541267.5:c.188_189insAAAAAAAAAAA	ENSP00000444434.1:p.Glu64LysfsTer?
NM_001297698.1:c.260_261insAAAAAAAAAAA	NP_001284627.1:p.Glu88LysfsTer?
NM_024865.3:c.260_261insAAAAAAAAAAA	NP_079141.2:p.Glu88LysfsTer?
XM_011520850.1:c.260_261insAAAAAAAAAAA	XP_011519152.1:p.Glu88LysfsTer?
XM_011520851.1:c.188_189insAAAAAAAAAAA	XP_011519153.1:p.Glu64LysfsTer?
XM_011520852.1:c.-113_-112insAAAAAAAAAAA	XP_011519154.1:n.-113_-112insAAAAAAAAAAA
NM_024865.4:c.260_261insAAAAAAAAAAA MANE Select	NP_079141.2:p.Glu88LysfsTer?
NM_001297698.2:c.260_261insAAAAAAAAAAA	NP_001284627.1:p.Glu88LysfsTer?