Canonical Allele Identifier: CA2014710344

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792920_7792922delinsCAA , CM000674.2:g.7792920_7792922delinsCAA	GRCh38
NC_000012.11:g.7945516_7945518delinsCAA , CM000674.1:g.7945516_7945518delinsCAA	GRCh37
NC_000012.10:g.7836783_7836785delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-30_152-28delinsCAA MANE Select	ENSP00000229307.4:n.152-30_152-28delinsCAA
ENST00000229307.8:c.152-30_152-28delinsCAA	ENSP00000229307.4:n.152-30_152-28delinsCAA
ENST00000526286.1:c.152-30_152-28delinsCAA	ENSP00000435288.1:n.152-30_152-28delinsCAA
ENST00000526434.2:n.334-68_334-66delinsCAA
ENST00000541267.5:c.80-30_80-28delinsCAA	ENSP00000444434.1:n.80-30_80-28delinsCAA
NM_001297698.1:c.152-30_152-28delinsCAA	NP_001284627.1:n.152-30_152-28delinsCAA
NM_024865.3:c.152-30_152-28delinsCAA	NP_079141.2:n.152-30_152-28delinsCAA
XM_011520850.1:c.152-30_152-28delinsCAA	XP_011519152.1:n.152-30_152-28delinsCAA
XM_011520851.1:c.80-30_80-28delinsCAA	XP_011519153.1:n.80-30_80-28delinsCAA
XM_011520852.1:c.-183-68_-183-66delinsCAA	XP_011519154.1:n.-183-68_-183-66delinsCAA
NM_024865.4:c.152-30_152-28delinsCAA MANE Select	NP_079141.2:n.152-30_152-28delinsCAA
NM_001297698.2:c.152-30_152-28delinsCAA	NP_001284627.1:n.152-30_152-28delinsCAA