Canonical Allele Identifier: CA2014710652

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793141C= , CM000674.2:g.7793141C=	GRCh38
NC_000012.11:g.7945737C= , CM000674.1:g.7945737C=	GRCh37
NC_000012.10:g.7837004C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.343C= MANE Select	ENSP00000229307.4:p.Gln115=
ENST00000229307.8:c.343C=	ENSP00000229307.4:p.Gln115=
ENST00000526286.1:c.343C=	ENSP00000435288.1:p.Gln115=
ENST00000526434.2:n.487C=
ENST00000541267.5:c.271C=	ENSP00000444434.1:p.Gln91=
NM_001297698.1:c.343C=	NP_001284627.1:p.Gln115=
NM_024865.3:c.343C=	NP_079141.2:p.Gln115=
XM_011520850.1:c.343C=	XP_011519152.1:p.Gln115=
XM_011520851.1:c.271C=	XP_011519153.1:p.Gln91=
XM_011520852.1:c.-30C=	XP_011519154.1:n.-30C=
NM_024865.4:c.343C= MANE Select	NP_079141.2:p.Gln115=
NM_001297698.2:c.343C=	NP_001284627.1:p.Gln115=