Canonical Allele Identifier: CA2014710259
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792828T= , CM000674.2:g.7792828T= GRCh38
NC_000012.11:g.7945424T= , CM000674.1:g.7945424T= GRCh37
NC_000012.10:g.7836691T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-122T= MANE Select ENSP00000229307.4:n.152-122T=
ENST00000229307.8:c.152-122T= ENSP00000229307.4:n.152-122T=
ENST00000526286.1:c.152-122T= ENSP00000435288.1:n.152-122T=
ENST00000526434.2:n.334-160T=
ENST00000541267.5:c.80-122T= ENSP00000444434.1:n.80-122T=
NM_001297698.1:c.152-122T= NP_001284627.1:n.152-122T=
NM_024865.3:c.152-122T= NP_079141.2:n.152-122T=
XM_011520850.1:c.152-122T= XP_011519152.1:n.152-122T=
XM_011520851.1:c.80-122T= XP_011519153.1:n.80-122T=
XM_011520852.1:c.-183-160T= XP_011519154.1:n.-183-160T=
NM_024865.4:c.152-122T= MANE Select NP_079141.2:n.152-122T=
NM_001297698.2:c.152-122T= NP_001284627.1:n.152-122T=