Canonical Allele Identifier: CA478527605

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945775A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793179A>G , CM000674.2:g.7793179A>G	GRCh38
NC_000012.11:g.7945775A>G , CM000674.1:g.7945775A>G	GRCh37
NC_000012.10:g.7837042A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.381A>G MANE Select	ENSP00000229307.4:p.Glu127=
ENST00000229307.8:c.381A>G	ENSP00000229307.4:p.Glu127=
ENST00000526286.1:c.381A>G	ENSP00000435288.1:p.Glu127=
ENST00000526434.2:n.525A>G
ENST00000541267.5:c.309A>G	ENSP00000444434.1:p.Glu103=
NM_001297698.1:c.381A>G	NP_001284627.1:p.Glu127=
NM_024865.3:c.381A>G	NP_079141.2:p.Glu127=
XM_011520850.1:c.381A>G	XP_011519152.1:p.Glu127=
XM_011520851.1:c.309A>G	XP_011519153.1:p.Glu103=
XM_011520852.1:c.9A>G	XP_011519154.1:p.Glu3=
NM_024865.4:c.381A>G MANE Select	NP_079141.2:p.Glu127=
NM_001297698.2:c.381A>G	NP_001284627.1:p.Glu127=