Canonical Allele Identifier: CA478527498

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945601C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793005C>T , CM000674.2:g.7793005C>T	GRCh38
NC_000012.11:g.7945601C>T , CM000674.1:g.7945601C>T	GRCh37
NC_000012.10:g.7836868C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.207C>T MANE Select	ENSP00000229307.4:p.Ser69=
ENST00000229307.8:c.207C>T	ENSP00000229307.4:p.Ser69=
ENST00000526286.1:c.207C>T	ENSP00000435288.1:p.Ser69=
ENST00000526434.2:n.351C>T
ENST00000541267.5:c.135C>T	ENSP00000444434.1:p.Ser45=
NM_001297698.1:c.207C>T	NP_001284627.1:p.Ser69=
NM_024865.3:c.207C>T	NP_079141.2:p.Ser69=
XM_011520850.1:c.207C>T	XP_011519152.1:p.Ser69=
XM_011520851.1:c.135C>T	XP_011519153.1:p.Ser45=
XM_011520852.1:c.-166C>T	XP_011519154.1:n.-166C>T
NM_024865.4:c.207C>T MANE Select	NP_079141.2:p.Ser69=
NM_001297698.2:c.207C>T	NP_001284627.1:p.Ser69=