Canonical Allele Identifier: CA383779946
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792974A>C , CM000674.2:g.7792974A>C GRCh38
NC_000012.11:g.7945570A>C , CM000674.1:g.7945570A>C GRCh37
NC_000012.10:g.7836837A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.176A>C MANE Select ENSP00000229307.4:p.Asp59Ala
ENST00000229307.8:c.176A>C ENSP00000229307.4:p.Asp59Ala
ENST00000526286.1:c.176A>C ENSP00000435288.1:p.Asp59Ala
ENST00000526434.2:n.334-14A>C
ENST00000541267.5:c.104A>C ENSP00000444434.1:p.Asp35Ala
NM_001297698.1:c.176A>C NP_001284627.1:p.Asp59Ala
NM_024865.3:c.176A>C NP_079141.2:p.Asp59Ala
XM_011520850.1:c.176A>C XP_011519152.1:p.Asp59Ala
XM_011520851.1:c.104A>C XP_011519153.1:p.Asp35Ala
XM_011520852.1:c.-183-14A>C XP_011519154.1:n.-183-14A>C
NM_024865.4:c.176A>C MANE Select NP_079141.2:p.Asp59Ala
NM_001297698.2:c.176A>C NP_001284627.1:p.Asp59Ala