Canonical Allele Identifier: CA692123467

Gene: NANOG

Linked Data

• dbSNP Id: rs1291264622
• MyVariant Identifiers: chr12:g.7945714_7945715del (hg19) ; chr12:g.7793118_7793119del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793123_7793124del , CM000674.2:g.7793123_7793124del	GRCh38
NC_000012.11:g.7945719_7945720del , CM000674.1:g.7945719_7945720del	GRCh37
NC_000012.10:g.7836986_7836987del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.325_326del MANE Select	ENSP00000229307.4:p.Val109ThrfsTer3
ENST00000229307.8:c.325_326del	ENSP00000229307.4:p.Val109ThrfsTer3
ENST00000526286.1:c.325_326del	ENSP00000435288.1:p.Val109ThrfsTer3
ENST00000526434.2:n.469_470del
ENST00000541267.5:c.253_254del	ENSP00000444434.1:p.Val85ThrfsTer3
NM_001297698.1:c.325_326del	NP_001284627.1:p.Val109ThrfsTer3
NM_024865.3:c.325_326del	NP_079141.2:p.Val109ThrfsTer3
XM_011520850.1:c.325_326del	XP_011519152.1:p.Val109ThrfsTer3
XM_011520851.1:c.253_254del	XP_011519153.1:p.Val85ThrfsTer3
XM_011520852.1:c.-48_-47del	XP_011519154.1:n.-48_-47del
NM_024865.4:c.325_326del MANE Select	NP_079141.2:p.Val109ThrfsTer3
NM_001297698.2:c.325_326del	NP_001284627.1:p.Val109ThrfsTer3