Canonical Allele Identifier: CA383780116
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793003T>A , CM000674.2:g.7793003T>A GRCh38
NC_000012.11:g.7945599T>A , CM000674.1:g.7945599T>A GRCh37
NC_000012.10:g.7836866T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.205T>A MANE Select ENSP00000229307.4:p.Ser69Thr
ENST00000229307.8:c.205T>A ENSP00000229307.4:p.Ser69Thr
ENST00000526286.1:c.205T>A ENSP00000435288.1:p.Ser69Thr
ENST00000526434.2:n.349T>A
ENST00000541267.5:c.133T>A ENSP00000444434.1:p.Ser45Thr
NM_001297698.1:c.205T>A NP_001284627.1:p.Ser69Thr
NM_024865.3:c.205T>A NP_079141.2:p.Ser69Thr
XM_011520850.1:c.205T>A XP_011519152.1:p.Ser69Thr
XM_011520851.1:c.133T>A XP_011519153.1:p.Ser45Thr
XM_011520852.1:c.-168T>A XP_011519154.1:n.-168T>A
NM_024865.4:c.205T>A MANE Select NP_079141.2:p.Ser69Thr
NM_001297698.2:c.205T>A NP_001284627.1:p.Ser69Thr