Canonical Allele Identifier: CA2014710664

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793155C= , CM000674.2:g.7793155C=	GRCh38
NC_000012.11:g.7945751C= , CM000674.1:g.7945751C=	GRCh37
NC_000012.10:g.7837018C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.357C= MANE Select	ENSP00000229307.4:p.Tyr119=
ENST00000229307.8:c.357C=	ENSP00000229307.4:p.Tyr119=
ENST00000526286.1:c.357C=	ENSP00000435288.1:p.Tyr119=
ENST00000526434.2:n.501C=
ENST00000541267.5:c.285C=	ENSP00000444434.1:p.Tyr95=
NM_001297698.1:c.357C=	NP_001284627.1:p.Tyr119=
NM_024865.3:c.357C=	NP_079141.2:p.Tyr119=
XM_011520850.1:c.357C=	XP_011519152.1:p.Tyr119=
XM_011520851.1:c.285C=	XP_011519153.1:p.Tyr95=
XM_011520852.1:c.-16C=	XP_011519154.1:n.-16C=
NM_024865.4:c.357C= MANE Select	NP_079141.2:p.Tyr119=
NM_001297698.2:c.357C=	NP_001284627.1:p.Tyr119=