Canonical Allele Identifier: CA383780079

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945590C>A (hg19) ; chr12:g.7792994C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792994C>A , CM000674.2:g.7792994C>A	GRCh38
NC_000012.11:g.7945590C>A , CM000674.1:g.7945590C>A	GRCh37
NC_000012.10:g.7836857C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.196C>A MANE Select	ENSP00000229307.4:p.Pro66Thr
ENST00000229307.8:c.196C>A	ENSP00000229307.4:p.Pro66Thr
ENST00000526286.1:c.196C>A	ENSP00000435288.1:p.Pro66Thr
ENST00000526434.2:n.340C>A
ENST00000541267.5:c.124C>A	ENSP00000444434.1:p.Pro42Thr
NM_001297698.1:c.196C>A	NP_001284627.1:p.Pro66Thr
NM_024865.3:c.196C>A	NP_079141.2:p.Pro66Thr
XM_011520850.1:c.196C>A	XP_011519152.1:p.Pro66Thr
XM_011520851.1:c.124C>A	XP_011519153.1:p.Pro42Thr
XM_011520852.1:c.-177C>A	XP_011519154.1:n.-177C>A
NM_024865.4:c.196C>A MANE Select	NP_079141.2:p.Pro66Thr
NM_001297698.2:c.196C>A	NP_001284627.1:p.Pro66Thr