Canonical Allele Identifier: CA2014710491

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793037C= , CM000674.2:g.7793037C=	GRCh38
NC_000012.11:g.7945633C= , CM000674.1:g.7945633C=	GRCh37
NC_000012.10:g.7836900C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.239C= MANE Select	ENSP00000229307.4:p.Ala80=
ENST00000229307.8:c.239C=	ENSP00000229307.4:p.Ala80=
ENST00000526286.1:c.239C=	ENSP00000435288.1:p.Ala80=
ENST00000526434.2:n.383C=
ENST00000541267.5:c.167C=	ENSP00000444434.1:p.Ala56=
NM_001297698.1:c.239C=	NP_001284627.1:p.Ala80=
NM_024865.3:c.239C=	NP_079141.2:p.Ala80=
XM_011520850.1:c.239C=	XP_011519152.1:p.Ala80=
XM_011520851.1:c.167C=	XP_011519153.1:p.Ala56=
XM_011520852.1:c.-134C=	XP_011519154.1:n.-134C=
NM_024865.4:c.239C= MANE Select	NP_079141.2:p.Ala80=
NM_001297698.2:c.239C=	NP_001284627.1:p.Ala80=