Canonical Allele Identifier: CA2014710198
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792741A= , CM000674.2:g.7792741A= GRCh38
NC_000012.11:g.7945337A= , CM000674.1:g.7945337A= GRCh37
NC_000012.10:g.7836604A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-209A= MANE Select ENSP00000229307.4:n.152-209A=
ENST00000229307.8:c.152-209A= ENSP00000229307.4:n.152-209A=
ENST00000526286.1:c.152-209A= ENSP00000435288.1:n.152-209A=
ENST00000526434.2:n.334-247A=
ENST00000541267.5:c.80-209A= ENSP00000444434.1:n.80-209A=
NM_001297698.1:c.152-209A= NP_001284627.1:n.152-209A=
NM_024865.3:c.152-209A= NP_079141.2:n.152-209A=
XM_011520850.1:c.152-209A= XP_011519152.1:n.152-209A=
XM_011520851.1:c.80-209A= XP_011519153.1:n.80-209A=
XM_011520852.1:c.-183-247A= XP_011519154.1:n.-183-247A=
NM_024865.4:c.152-209A= MANE Select NP_079141.2:n.152-209A=
NM_001297698.2:c.152-209A= NP_001284627.1:n.152-209A=