Canonical Allele Identifier: CA478527539
Gene: NANOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.7945649A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793053A>C , CM000674.2:g.7793053A>C GRCh38
NC_000012.11:g.7945649A>C , CM000674.1:g.7945649A>C GRCh37
NC_000012.10:g.7836916A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.255A>C MANE Select ENSP00000229307.4:p.Ala85=
ENST00000229307.8:c.255A>C ENSP00000229307.4:p.Ala85=
ENST00000526286.1:c.255A>C ENSP00000435288.1:p.Ala85=
ENST00000526434.2:n.399A>C
ENST00000541267.5:c.183A>C ENSP00000444434.1:p.Ala61=
NM_001297698.1:c.255A>C NP_001284627.1:p.Ala85=
NM_024865.3:c.255A>C NP_079141.2:p.Ala85=
XM_011520850.1:c.255A>C XP_011519152.1:p.Ala85=
XM_011520851.1:c.183A>C XP_011519153.1:p.Ala61=
XM_011520852.1:c.-118A>C XP_011519154.1:n.-118A>C
NM_024865.4:c.255A>C MANE Select NP_079141.2:p.Ala85=
NM_001297698.2:c.255A>C NP_001284627.1:p.Ala85=