Canonical Allele Identifier: CA2014710250
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792823T= , CM000674.2:g.7792823T= GRCh38
NC_000012.11:g.7945419T= , CM000674.1:g.7945419T= GRCh37
NC_000012.10:g.7836686T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-127T= MANE Select ENSP00000229307.4:n.152-127T=
ENST00000229307.8:c.152-127T= ENSP00000229307.4:n.152-127T=
ENST00000526286.1:c.152-127T= ENSP00000435288.1:n.152-127T=
ENST00000526434.2:n.334-165T=
ENST00000541267.5:c.80-127T= ENSP00000444434.1:n.80-127T=
NM_001297698.1:c.152-127T= NP_001284627.1:n.152-127T=
NM_024865.3:c.152-127T= NP_079141.2:n.152-127T=
XM_011520850.1:c.152-127T= XP_011519152.1:n.152-127T=
XM_011520851.1:c.80-127T= XP_011519153.1:n.80-127T=
XM_011520852.1:c.-183-165T= XP_011519154.1:n.-183-165T=
NM_024865.4:c.152-127T= MANE Select NP_079141.2:n.152-127T=
NM_001297698.2:c.152-127T= NP_001284627.1:n.152-127T=