Canonical Allele Identifier: CA6429984

Gene: NANOG

Linked Data

• dbSNP Id: rs763289367
• ExAC: 12:7945726 A / G
• gnomAD v2: 12-7945726-A-G
• gnomAD v3: 12-7793130-A-G
• gnomAD v4: 12-7793130-A-G
• MyVariant Identifiers: chr12:g.7945726A>G (hg19) ; chr12:g.7793130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793130A>G , CM000674.2:g.7793130A>G	GRCh38
NC_000012.11:g.7945726A>G , CM000674.1:g.7945726A>G	GRCh37
NC_000012.10:g.7836993A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.332A>G MANE Select	ENSP00000229307.4:p.Asn111Ser
ENST00000229307.8:c.332A>G	ENSP00000229307.4:p.Asn111Ser
ENST00000526286.1:c.332A>G	ENSP00000435288.1:p.Asn111Ser
ENST00000526434.2:n.476A>G
ENST00000541267.5:c.260A>G	ENSP00000444434.1:p.Asn87Ser
NM_001297698.1:c.332A>G	NP_001284627.1:p.Asn111Ser
NM_024865.3:c.332A>G	NP_079141.2:p.Asn111Ser
XM_011520850.1:c.332A>G	XP_011519152.1:p.Asn111Ser
XM_011520851.1:c.260A>G	XP_011519153.1:p.Asn87Ser
XM_011520852.1:c.-41A>G	XP_011519154.1:n.-41A>G
NM_024865.4:c.332A>G MANE Select	NP_079141.2:p.Asn111Ser
NM_001297698.2:c.332A>G	NP_001284627.1:p.Asn111Ser