Canonical Allele Identifier: CA944452998

Gene: NANOG

Linked Data

• gnomAD v3: 12-7792600-G-GGAGT
• gnomAD v4: 12-7792600-G-GGAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792600_7792601insGAGT , CM000674.2:g.7792600_7792601insGAGT	GRCh38
NC_000012.11:g.7945196_7945197insGAGT , CM000674.1:g.7945196_7945197insGAGT	GRCh37
NC_000012.10:g.7836463_7836464insGAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-350_152-349insGAGT MANE Select	ENSP00000229307.4:n.152-350_152-349insGAGT
ENST00000229307.8:c.152-350_152-349insGAGT	ENSP00000229307.4:n.152-350_152-349insGAGT
ENST00000526286.1:c.152-350_152-349insGAGT	ENSP00000435288.1:n.152-350_152-349insGAGT
ENST00000526434.2:n.334-388_334-387insGAGT
ENST00000541267.5:c.80-350_80-349insGAGT	ENSP00000444434.1:n.80-350_80-349insGAGT
NM_001297698.1:c.152-350_152-349insGAGT	NP_001284627.1:n.152-350_152-349insGAGT
NM_024865.3:c.152-350_152-349insGAGT	NP_079141.2:n.152-350_152-349insGAGT
XM_011520850.1:c.152-350_152-349insGAGT	XP_011519152.1:n.152-350_152-349insGAGT
XM_011520851.1:c.80-350_80-349insGAGT	XP_011519153.1:n.80-350_80-349insGAGT
XM_011520852.1:c.-183-388_-183-387insGAGT	XP_011519154.1:n.-183-388_-183-387insGAGT
NM_024865.4:c.152-350_152-349insGAGT MANE Select	NP_079141.2:n.152-350_152-349insGAGT
NM_001297698.2:c.152-350_152-349insGAGT	NP_001284627.1:n.152-350_152-349insGAGT