Canonical Allele Identifier: CA2014710581

Gene: NANOG

Linked Data

• dbSNP Id: rs1862865352

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793091_7793093dup , CM000674.2:g.7793091_7793093dup	GRCh38
NC_000012.11:g.7945687_7945689dup , CM000674.1:g.7945687_7945689dup	GRCh37
NC_000012.10:g.7836954_7836956dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.293_295dup MANE Select	ENSP00000229307.4:p.Thr98_Arg99insThr
ENST00000229307.8:c.293_295dup	ENSP00000229307.4:p.Thr98_Arg99insThr
ENST00000526286.1:c.293_295dup	ENSP00000435288.1:p.Thr98_Arg99insThr
ENST00000526434.2:n.437_439dup
ENST00000541267.5:c.221_223dup	ENSP00000444434.1:p.Thr74_Arg75insThr
NM_001297698.1:c.293_295dup	NP_001284627.1:p.Thr98_Arg99insThr
NM_024865.3:c.293_295dup	NP_079141.2:p.Thr98_Arg99insThr
XM_011520850.1:c.293_295dup	XP_011519152.1:p.Thr98_Arg99insThr
XM_011520851.1:c.221_223dup	XP_011519153.1:p.Thr74_Arg75insThr
XM_011520852.1:c.-80_-78dup	XP_011519154.1:n.-80_-78dup
NM_024865.4:c.293_295dup MANE Select	NP_079141.2:p.Thr98_Arg99insThr
NM_001297698.2:c.293_295dup	NP_001284627.1:p.Thr98_Arg99insThr