Canonical Allele Identifier: CA6429971

Gene: NANOG

Linked Data

• dbSNP Id: rs767551668
• ExAC: 12:7945647 G / A
• gnomAD v2: 12-7945647-G-A
• gnomAD v3: 12-7793051-G-A
• gnomAD v4: 12-7793051-G-A
• COSMIC: COSM5108691
• MyVariant Identifiers: chr12:g.7945647G>A (hg19) ; chr12:g.7793051G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793051G>A , CM000674.2:g.7793051G>A	GRCh38
NC_000012.11:g.7945647G>A , CM000674.1:g.7945647G>A	GRCh37
NC_000012.10:g.7836914G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.253G>A MANE Select	ENSP00000229307.4:p.Ala85Thr
ENST00000229307.8:c.253G>A	ENSP00000229307.4:p.Ala85Thr
ENST00000526286.1:c.253G>A	ENSP00000435288.1:p.Ala85Thr
ENST00000526434.2:n.397G>A
ENST00000541267.5:c.181G>A	ENSP00000444434.1:p.Ala61Thr
NM_001297698.1:c.253G>A	NP_001284627.1:p.Ala85Thr
NM_024865.3:c.253G>A	NP_079141.2:p.Ala85Thr
XM_011520850.1:c.253G>A	XP_011519152.1:p.Ala85Thr
XM_011520851.1:c.181G>A	XP_011519153.1:p.Ala61Thr
XM_011520852.1:c.-120G>A	XP_011519154.1:n.-120G>A
NM_024865.4:c.253G>A MANE Select	NP_079141.2:p.Ala85Thr
NM_001297698.2:c.253G>A	NP_001284627.1:p.Ala85Thr