Canonical Allele Identifier: CA2014710124

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792670_7792671delinsTA , CM000674.2:g.7792670_7792671delinsTA	GRCh38
NC_000012.11:g.7945266_7945267delinsTA , CM000674.1:g.7945266_7945267delinsTA	GRCh37
NC_000012.10:g.7836533_7836534delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-280_152-279delinsTA MANE Select	ENSP00000229307.4:n.152-280_152-279delinsTA
ENST00000229307.8:c.152-280_152-279delinsTA	ENSP00000229307.4:n.152-280_152-279delinsTA
ENST00000526286.1:c.152-280_152-279delinsTA	ENSP00000435288.1:n.152-280_152-279delinsTA
ENST00000526434.2:n.334-318_334-317delinsTA
ENST00000541267.5:c.80-280_80-279delinsTA	ENSP00000444434.1:n.80-280_80-279delinsTA
NM_001297698.1:c.152-280_152-279delinsTA	NP_001284627.1:n.152-280_152-279delinsTA
NM_024865.3:c.152-280_152-279delinsTA	NP_079141.2:n.152-280_152-279delinsTA
XM_011520850.1:c.152-280_152-279delinsTA	XP_011519152.1:n.152-280_152-279delinsTA
XM_011520851.1:c.80-280_80-279delinsTA	XP_011519153.1:n.80-280_80-279delinsTA
XM_011520852.1:c.-183-318_-183-317delinsTA	XP_011519154.1:n.-183-318_-183-317delinsTA
NM_024865.4:c.152-280_152-279delinsTA MANE Select	NP_079141.2:n.152-280_152-279delinsTA
NM_001297698.2:c.152-280_152-279delinsTA	NP_001284627.1:n.152-280_152-279delinsTA