Canonical Allele Identifier: CA383779900

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945563T>A (hg19) ; chr12:g.7792967T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792967T>A , CM000674.2:g.7792967T>A	GRCh38
NC_000012.11:g.7945563T>A , CM000674.1:g.7945563T>A	GRCh37
NC_000012.10:g.7836830T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.169T>A MANE Select	ENSP00000229307.4:p.Ser57Thr
ENST00000229307.8:c.169T>A	ENSP00000229307.4:p.Ser57Thr
ENST00000526286.1:c.169T>A	ENSP00000435288.1:p.Ser57Thr
ENST00000526434.2:n.334-21T>A
ENST00000541267.5:c.97T>A	ENSP00000444434.1:p.Ser33Thr
NM_001297698.1:c.169T>A	NP_001284627.1:p.Ser57Thr
NM_024865.3:c.169T>A	NP_079141.2:p.Ser57Thr
XM_011520850.1:c.169T>A	XP_011519152.1:p.Ser57Thr
XM_011520851.1:c.97T>A	XP_011519153.1:p.Ser33Thr
XM_011520852.1:c.-183-21T>A	XP_011519154.1:n.-183-21T>A
NM_024865.4:c.169T>A MANE Select	NP_079141.2:p.Ser57Thr
NM_001297698.2:c.169T>A	NP_001284627.1:p.Ser57Thr