Canonical Allele Identifier: CA2014710136

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792676_7792679delinsAAAG , CM000674.2:g.7792676_7792679delinsAAAG	GRCh38
NC_000012.11:g.7945272_7945275delinsAAAG , CM000674.1:g.7945272_7945275delinsAAAG	GRCh37
NC_000012.10:g.7836539_7836542delinsAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-274_152-271delinsAAAG MANE Select	ENSP00000229307.4:n.152-274_152-271delinsAAAG
ENST00000229307.8:c.152-274_152-271delinsAAAG	ENSP00000229307.4:n.152-274_152-271delinsAAAG
ENST00000526286.1:c.152-274_152-271delinsAAAG	ENSP00000435288.1:n.152-274_152-271delinsAAAG
ENST00000526434.2:n.334-312_334-309delinsAAAG
ENST00000541267.5:c.80-274_80-271delinsAAAG	ENSP00000444434.1:n.80-274_80-271delinsAAAG
NM_001297698.1:c.152-274_152-271delinsAAAG	NP_001284627.1:n.152-274_152-271delinsAAAG
NM_024865.3:c.152-274_152-271delinsAAAG	NP_079141.2:n.152-274_152-271delinsAAAG
XM_011520850.1:c.152-274_152-271delinsAAAG	XP_011519152.1:n.152-274_152-271delinsAAAG
XM_011520851.1:c.80-274_80-271delinsAAAG	XP_011519153.1:n.80-274_80-271delinsAAAG
XM_011520852.1:c.-183-312_-183-309delinsAAAG	XP_011519154.1:n.-183-312_-183-309delinsAAAG
NM_024865.4:c.152-274_152-271delinsAAAG MANE Select	NP_079141.2:n.152-274_152-271delinsAAAG
NM_001297698.2:c.152-274_152-271delinsAAAG	NP_001284627.1:n.152-274_152-271delinsAAAG