Canonical Allele Identifier: CA383780529
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793060G>C , CM000674.2:g.7793060G>C GRCh38
NC_000012.11:g.7945656G>C , CM000674.1:g.7945656G>C GRCh37
NC_000012.10:g.7836923G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.262G>C MANE Select ENSP00000229307.4:p.Glu88Gln
ENST00000229307.8:c.262G>C ENSP00000229307.4:p.Glu88Gln
ENST00000526286.1:c.262G>C ENSP00000435288.1:p.Glu88Gln
ENST00000526434.2:n.406G>C
ENST00000541267.5:c.190G>C ENSP00000444434.1:p.Glu64Gln
NM_001297698.1:c.262G>C NP_001284627.1:p.Glu88Gln
NM_024865.3:c.262G>C NP_079141.2:p.Glu88Gln
XM_011520850.1:c.262G>C XP_011519152.1:p.Glu88Gln
XM_011520851.1:c.190G>C XP_011519153.1:p.Glu64Gln
XM_011520852.1:c.-111G>C XP_011519154.1:n.-111G>C
NM_024865.4:c.262G>C MANE Select NP_079141.2:p.Glu88Gln
NM_001297698.2:c.262G>C NP_001284627.1:p.Glu88Gln