Canonical Allele Identifier: CA478527482

Gene: NANOG

Linked Data

• COSMIC: COSM391468
• MyVariant Identifiers: chr12:g.7945589del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792995del , CM000674.2:g.7792995del	GRCh38
NC_000012.11:g.7945591del , CM000674.1:g.7945591del	GRCh37
NC_000012.10:g.7836858del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.197del MANE Select	ENSP00000229307.4:p.Pro66LeufsTer?
ENST00000229307.8:c.197del	ENSP00000229307.4:p.Pro66LeufsTer?
ENST00000526286.1:c.197del	ENSP00000435288.1:p.Pro66LeufsTer?
ENST00000526434.2:n.341del
ENST00000541267.5:c.125del	ENSP00000444434.1:p.Pro42LeufsTer?
NM_001297698.1:c.197del	NP_001284627.1:p.Pro66LeufsTer?
NM_024865.3:c.197del	NP_079141.2:p.Pro66LeufsTer?
XM_011520850.1:c.197del	XP_011519152.1:p.Pro66LeufsTer?
XM_011520851.1:c.125del	XP_011519153.1:p.Pro42LeufsTer?
XM_011520852.1:c.-176del	XP_011519154.1:n.-176del
NM_024865.4:c.197del MANE Select	NP_079141.2:p.Pro66LeufsTer?
NM_001297698.2:c.197del	NP_001284627.1:p.Pro66LeufsTer?