Canonical Allele Identifier: CA383780984
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1444900069

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793132G>T , CM000674.2:g.7793132G>T GRCh38
NC_000012.11:g.7945728G>T , CM000674.1:g.7945728G>T GRCh37
NC_000012.10:g.7836995G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.334G>T MANE Select ENSP00000229307.4:p.Asp112Tyr
ENST00000229307.8:c.334G>T ENSP00000229307.4:p.Asp112Tyr
ENST00000526286.1:c.334G>T ENSP00000435288.1:p.Asp112Tyr
ENST00000526434.2:n.478G>T
ENST00000541267.5:c.262G>T ENSP00000444434.1:p.Asp88Tyr
NM_001297698.1:c.334G>T NP_001284627.1:p.Asp112Tyr
NM_024865.3:c.334G>T NP_079141.2:p.Asp112Tyr
XM_011520850.1:c.334G>T XP_011519152.1:p.Asp112Tyr
XM_011520851.1:c.262G>T XP_011519153.1:p.Asp88Tyr
XM_011520852.1:c.-39G>T XP_011519154.1:n.-39G>T
NM_024865.4:c.334G>T MANE Select NP_079141.2:p.Asp112Tyr
NM_001297698.2:c.334G>T NP_001284627.1:p.Asp112Tyr