Canonical Allele Identifier: CA2014710607

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793112C= , CM000674.2:g.7793112C=	GRCh38
NC_000012.11:g.7945708C= , CM000674.1:g.7945708C=	GRCh37
NC_000012.10:g.7836975C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.314C= MANE Select	ENSP00000229307.4:p.Thr105=
ENST00000229307.8:c.314C=	ENSP00000229307.4:p.Thr105=
ENST00000526286.1:c.314C=	ENSP00000435288.1:p.Thr105=
ENST00000526434.2:n.458C=
ENST00000541267.5:c.242C=	ENSP00000444434.1:p.Thr81=
NM_001297698.1:c.314C=	NP_001284627.1:p.Thr105=
NM_024865.3:c.314C=	NP_079141.2:p.Thr105=
XM_011520850.1:c.314C=	XP_011519152.1:p.Thr105=
XM_011520851.1:c.242C=	XP_011519153.1:p.Thr81=
XM_011520852.1:c.-59C=	XP_011519154.1:n.-59C=
NM_024865.4:c.314C= MANE Select	NP_079141.2:p.Thr105=
NM_001297698.2:c.314C=	NP_001284627.1:p.Thr105=