Canonical Allele Identifier: CA2617437545

Gene: NANOG

Linked Data

• gnomAD v4: 12-7793052-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793058del , CM000674.2:g.7793058del	GRCh38
NC_000012.11:g.7945654del , CM000674.1:g.7945654del	GRCh37
NC_000012.10:g.7836921del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.260del MANE Select	ENSP00000229307.4:p.Lys87ArgfsTer?
ENST00000229307.8:c.260del	ENSP00000229307.4:p.Lys87ArgfsTer?
ENST00000526286.1:c.260del	ENSP00000435288.1:p.Lys87ArgfsTer?
ENST00000526434.2:n.404del
ENST00000541267.5:c.188del	ENSP00000444434.1:p.Lys63ArgfsTer?
NM_001297698.1:c.260del	NP_001284627.1:p.Lys87ArgfsTer?
NM_024865.3:c.260del	NP_079141.2:p.Lys87ArgfsTer?
XM_011520850.1:c.260del	XP_011519152.1:p.Lys87ArgfsTer?
XM_011520851.1:c.188del	XP_011519153.1:p.Lys63ArgfsTer?
XM_011520852.1:c.-113del	XP_011519154.1:n.-113del
NM_024865.4:c.260del MANE Select	NP_079141.2:p.Lys87ArgfsTer?
NM_001297698.2:c.260del	NP_001284627.1:p.Lys87ArgfsTer?