Canonical Allele Identifier: CA692122951

Gene: NANOG

Linked Data

• dbSNP Id: rs1408055457
• gnomAD v3: 12-7792848-GTTCTGGGAATTATCAAAGTACTTTGAAAACAATTTTTTTAAAGGATAT-G
• gnomAD v4: 12-7792848-GTTCTGGGAATTATCAAAGTACTTTGAAAACAATTTTTTTAAAGGATAT-G
• MyVariant Identifiers: chr12:g.7945445_7945492del (hg19) ; chr12:g.7792849_7792896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792851_7792898del , CM000674.2:g.7792851_7792898del	GRCh38
NC_000012.11:g.7945447_7945494del , CM000674.1:g.7945447_7945494del	GRCh37
NC_000012.10:g.7836714_7836761del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-99_152-52del MANE Select	ENSP00000229307.4:n.152-99_152-52del
ENST00000229307.8:c.152-99_152-52del	ENSP00000229307.4:n.152-99_152-52del
ENST00000526286.1:c.152-99_152-52del	ENSP00000435288.1:n.152-99_152-52del
ENST00000526434.2:n.334-137_334-90del
ENST00000541267.5:c.80-99_80-52del	ENSP00000444434.1:n.80-99_80-52del
NM_001297698.1:c.152-99_152-52del	NP_001284627.1:n.152-99_152-52del
NM_024865.3:c.152-99_152-52del	NP_079141.2:n.152-99_152-52del
XM_011520850.1:c.152-99_152-52del	XP_011519152.1:n.152-99_152-52del
XM_011520851.1:c.80-99_80-52del	XP_011519153.1:n.80-99_80-52del
XM_011520852.1:c.-183-137_-183-90del	XP_011519154.1:n.-183-137_-183-90del
NM_024865.4:c.152-99_152-52del MANE Select	NP_079141.2:n.152-99_152-52del
NM_001297698.2:c.152-99_152-52del	NP_001284627.1:n.152-99_152-52del