Canonical Allele Identifier: CA2014710299

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792861T= , CM000674.2:g.7792861T=	GRCh38
NC_000012.11:g.7945457T= , CM000674.1:g.7945457T=	GRCh37
NC_000012.10:g.7836724T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-89T= MANE Select	ENSP00000229307.4:n.152-89T=
ENST00000229307.8:c.152-89T=	ENSP00000229307.4:n.152-89T=
ENST00000526286.1:c.152-89T=	ENSP00000435288.1:n.152-89T=
ENST00000526434.2:n.334-127T=
ENST00000541267.5:c.80-89T=	ENSP00000444434.1:n.80-89T=
NM_001297698.1:c.152-89T=	NP_001284627.1:n.152-89T=
NM_024865.3:c.152-89T=	NP_079141.2:n.152-89T=
XM_011520850.1:c.152-89T=	XP_011519152.1:n.152-89T=
XM_011520851.1:c.80-89T=	XP_011519153.1:n.80-89T=
XM_011520852.1:c.-183-127T=	XP_011519154.1:n.-183-127T=
NM_024865.4:c.152-89T= MANE Select	NP_079141.2:n.152-89T=
NM_001297698.2:c.152-89T=	NP_001284627.1:n.152-89T=