Canonical Allele Identifier: CA2575068018

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793080_7793082del , CM000674.2:g.7793080_7793082del	GRCh38
NC_000012.11:g.7945676_7945678del , CM000674.1:g.7945676_7945678del	GRCh37
NC_000012.10:g.7836943_7836945del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.282_284del MANE Select	ENSP00000229307.4:p.Lys95del
ENST00000229307.8:c.282_284del	ENSP00000229307.4:p.Lys95del
ENST00000526286.1:c.282_284del	ENSP00000435288.1:p.Lys95del
ENST00000526434.2:n.426_428del
ENST00000541267.5:c.210_212del	ENSP00000444434.1:p.Lys71del
NM_001297698.1:c.282_284del	NP_001284627.1:p.Lys95del
NM_024865.3:c.282_284del	NP_079141.2:p.Lys95del
XM_011520850.1:c.282_284del	XP_011519152.1:p.Lys95del
XM_011520851.1:c.210_212del	XP_011519153.1:p.Lys71del
XM_011520852.1:c.-91_-89del	XP_011519154.1:n.-91_-89del
NM_024865.4:c.282_284del MANE Select	NP_079141.2:p.Lys95del
NM_001297698.2:c.282_284del	NP_001284627.1:p.Lys95del