Canonical Allele Identifier: CA2014710480
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793030A= , CM000674.2:g.7793030A= GRCh38
NC_000012.11:g.7945626A= , CM000674.1:g.7945626A= GRCh37
NC_000012.10:g.7836893A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.232A= MANE Select ENSP00000229307.4:p.Thr78=
ENST00000229307.8:c.232A= ENSP00000229307.4:p.Thr78=
ENST00000526286.1:c.232A= ENSP00000435288.1:p.Thr78=
ENST00000526434.2:n.376A=
ENST00000541267.5:c.160A= ENSP00000444434.1:p.Thr54=
NM_001297698.1:c.232A= NP_001284627.1:p.Thr78=
NM_024865.3:c.232A= NP_079141.2:p.Thr78=
XM_011520850.1:c.232A= XP_011519152.1:p.Thr78=
XM_011520851.1:c.160A= XP_011519153.1:p.Thr54=
XM_011520852.1:c.-141A= XP_011519154.1:n.-141A=
NM_024865.4:c.232A= MANE Select NP_079141.2:p.Thr78=
NM_001297698.2:c.232A= NP_001284627.1:p.Thr78=