Canonical Allele Identifier: CA944452983

Gene: NANOG

Linked Data

• dbSNP Id: rs1862855642
• gnomAD v3: 12-7792561-G-GGCTGAGGCAGGAGAATCGCTTGAA
• gnomAD v4: 12-7792561-G-GGCTGAGGCAGGAGAATCGCTTGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792562_7792585dup , CM000674.2:g.7792562_7792585dup	GRCh38
NC_000012.11:g.7945158_7945181dup , CM000674.1:g.7945158_7945181dup	GRCh37
NC_000012.10:g.7836425_7836448dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-388_152-365dup MANE Select	ENSP00000229307.4:n.152-388_152-365dup
ENST00000229307.8:c.152-388_152-365dup	ENSP00000229307.4:n.152-388_152-365dup
ENST00000526286.1:c.152-388_152-365dup	ENSP00000435288.1:n.152-388_152-365dup
ENST00000526434.2:n.334-426_334-403dup
ENST00000541267.5:c.80-388_80-365dup	ENSP00000444434.1:n.80-388_80-365dup
NM_001297698.1:c.152-388_152-365dup	NP_001284627.1:n.152-388_152-365dup
NM_024865.3:c.152-388_152-365dup	NP_079141.2:n.152-388_152-365dup
XM_011520850.1:c.152-388_152-365dup	XP_011519152.1:n.152-388_152-365dup
XM_011520851.1:c.80-388_80-365dup	XP_011519153.1:n.80-388_80-365dup
XM_011520852.1:c.-183-426_-183-403dup	XP_011519154.1:n.-183-426_-183-403dup
NM_024865.4:c.152-388_152-365dup MANE Select	NP_079141.2:n.152-388_152-365dup
NM_001297698.2:c.152-388_152-365dup	NP_001284627.1:n.152-388_152-365dup