Canonical Allele Identifier: CA383780298
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793025A>T , CM000674.2:g.7793025A>T GRCh38
NC_000012.11:g.7945621A>T , CM000674.1:g.7945621A>T GRCh37
NC_000012.10:g.7836888A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.227A>T MANE Select ENSP00000229307.4:p.Gln76Leu
ENST00000229307.8:c.227A>T ENSP00000229307.4:p.Gln76Leu
ENST00000526286.1:c.227A>T ENSP00000435288.1:p.Gln76Leu
ENST00000526434.2:n.371A>T
ENST00000541267.5:c.155A>T ENSP00000444434.1:p.Gln52Leu
NM_001297698.1:c.227A>T NP_001284627.1:p.Gln76Leu
NM_024865.3:c.227A>T NP_079141.2:p.Gln76Leu
XM_011520850.1:c.227A>T XP_011519152.1:p.Gln76Leu
XM_011520851.1:c.155A>T XP_011519153.1:p.Gln52Leu
XM_011520852.1:c.-146A>T XP_011519154.1:n.-146A>T
NM_024865.4:c.227A>T MANE Select NP_079141.2:p.Gln76Leu
NM_001297698.2:c.227A>T NP_001284627.1:p.Gln76Leu