Canonical Allele Identifier: CA383780535
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793061A>T , CM000674.2:g.7793061A>T GRCh38
NC_000012.11:g.7945657A>T , CM000674.1:g.7945657A>T GRCh37
NC_000012.10:g.7836924A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.263A>T MANE Select ENSP00000229307.4:p.Glu88Val
ENST00000229307.8:c.263A>T ENSP00000229307.4:p.Glu88Val
ENST00000526286.1:c.263A>T ENSP00000435288.1:p.Glu88Val
ENST00000526434.2:n.407A>T
ENST00000541267.5:c.191A>T ENSP00000444434.1:p.Glu64Val
NM_001297698.1:c.263A>T NP_001284627.1:p.Glu88Val
NM_024865.3:c.263A>T NP_079141.2:p.Glu88Val
XM_011520850.1:c.263A>T XP_011519152.1:p.Glu88Val
XM_011520851.1:c.191A>T XP_011519153.1:p.Glu64Val
XM_011520852.1:c.-110A>T XP_011519154.1:n.-110A>T
NM_024865.4:c.263A>T MANE Select NP_079141.2:p.Glu88Val
NM_001297698.2:c.263A>T NP_001284627.1:p.Glu88Val