Canonical Allele Identifier: CA2014710613

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793117_7793119delinsCTG , CM000674.2:g.7793117_7793119delinsCTG	GRCh38
NC_000012.11:g.7945713_7945715delinsCTG , CM000674.1:g.7945713_7945715delinsCTG	GRCh37
NC_000012.10:g.7836980_7836982delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.319_321delinsCTG MANE Select	ENSP00000229307.4:p.Leu107=
ENST00000229307.8:c.319_321delinsCTG	ENSP00000229307.4:p.Leu107=
ENST00000526286.1:c.319_321delinsCTG	ENSP00000435288.1:p.Leu107=
ENST00000526434.2:n.463_465delinsCTG
ENST00000541267.5:c.247_249delinsCTG	ENSP00000444434.1:p.Leu83=
NM_001297698.1:c.319_321delinsCTG	NP_001284627.1:p.Leu107=
NM_024865.3:c.319_321delinsCTG	NP_079141.2:p.Leu107=
XM_011520850.1:c.319_321delinsCTG	XP_011519152.1:p.Leu107=
XM_011520851.1:c.247_249delinsCTG	XP_011519153.1:p.Leu83=
XM_011520852.1:c.-54_-52delinsCTG	XP_011519154.1:n.-54_-52delinsCTG
NM_024865.4:c.319_321delinsCTG MANE Select	NP_079141.2:p.Leu107=
NM_001297698.2:c.319_321delinsCTG	NP_001284627.1:p.Leu107=