Canonical Allele Identifier: CA383780425
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1414927275
gnomAD v2: 12-7945642-G-A
gnomAD v4: 12-7793046-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793046G>A , CM000674.2:g.7793046G>A GRCh38
NC_000012.11:g.7945642G>A , CM000674.1:g.7945642G>A GRCh37
NC_000012.10:g.7836909G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.248G>A MANE Select ENSP00000229307.4:p.Ser83Asn
ENST00000229307.8:c.248G>A ENSP00000229307.4:p.Ser83Asn
ENST00000526286.1:c.248G>A ENSP00000435288.1:p.Ser83Asn
ENST00000526434.2:n.392G>A
ENST00000541267.5:c.176G>A ENSP00000444434.1:p.Ser59Asn
NM_001297698.1:c.248G>A NP_001284627.1:p.Ser83Asn
NM_024865.3:c.248G>A NP_079141.2:p.Ser83Asn
XM_011520850.1:c.248G>A XP_011519152.1:p.Ser83Asn
XM_011520851.1:c.176G>A XP_011519153.1:p.Ser59Asn
XM_011520852.1:c.-125G>A XP_011519154.1:n.-125G>A
NM_024865.4:c.248G>A MANE Select NP_079141.2:p.Ser83Asn
NM_001297698.2:c.248G>A NP_001284627.1:p.Ser83Asn