Canonical Allele Identifier: CA383780553

Gene: NANOG

Linked Data

• gnomAD v4: 12-7793064-A-G
• MyVariant Identifiers: chr12:g.7945660A>G (hg19) ; chr12:g.7793064A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793064A>G , CM000674.2:g.7793064A>G	GRCh38
NC_000012.11:g.7945660A>G , CM000674.1:g.7945660A>G	GRCh37
NC_000012.10:g.7836927A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.266A>G MANE Select	ENSP00000229307.4:p.Asp89Gly
ENST00000229307.8:c.266A>G	ENSP00000229307.4:p.Asp89Gly
ENST00000526286.1:c.266A>G	ENSP00000435288.1:p.Asp89Gly
ENST00000526434.2:n.410A>G
ENST00000541267.5:c.194A>G	ENSP00000444434.1:p.Asp65Gly
NM_001297698.1:c.266A>G	NP_001284627.1:p.Asp89Gly
NM_024865.3:c.266A>G	NP_079141.2:p.Asp89Gly
XM_011520850.1:c.266A>G	XP_011519152.1:p.Asp89Gly
XM_011520851.1:c.194A>G	XP_011519153.1:p.Asp65Gly
XM_011520852.1:c.-107A>G	XP_011519154.1:n.-107A>G
NM_024865.4:c.266A>G MANE Select	NP_079141.2:p.Asp89Gly
NM_001297698.2:c.266A>G	NP_001284627.1:p.Asp89Gly