Canonical Allele Identifier: CA6429992

Gene: NANOG

Linked Data

• dbSNP Id: rs753791059
• ExAC: 12:7945779 T / G
• gnomAD v2: 12-7945779-T-G
• gnomAD v4: 12-7793183-T-G
• MyVariant Identifiers: chr12:g.7945779T>G (hg19) ; chr12:g.7793183T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793183T>G , CM000674.2:g.7793183T>G	GRCh38
NC_000012.11:g.7945779T>G , CM000674.1:g.7945779T>G	GRCh37
NC_000012.10:g.7837046T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.385T>G MANE Select	ENSP00000229307.4:p.Ser129Ala
ENST00000229307.8:c.385T>G	ENSP00000229307.4:p.Ser129Ala
ENST00000526286.1:c.385T>G	ENSP00000435288.1:p.Ser129Ala
ENST00000526434.2:n.529T>G
ENST00000541267.5:c.313T>G	ENSP00000444434.1:p.Ser105Ala
NM_001297698.1:c.385T>G	NP_001284627.1:p.Ser129Ala
NM_024865.3:c.385T>G	NP_079141.2:p.Ser129Ala
XM_011520850.1:c.385T>G	XP_011519152.1:p.Ser129Ala
XM_011520851.1:c.313T>G	XP_011519153.1:p.Ser105Ala
XM_011520852.1:c.13T>G	XP_011519154.1:p.Ser5Ala
NM_024865.4:c.385T>G MANE Select	NP_079141.2:p.Ser129Ala
NM_001297698.2:c.385T>G	NP_001284627.1:p.Ser129Ala