Canonical Allele Identifier: CA383780682
Gene: NANOG HGNC NCBI

Linked Data

gnomAD v4: 12-7793083-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793083A>T , CM000674.2:g.7793083A>T GRCh38
NC_000012.11:g.7945679A>T , CM000674.1:g.7945679A>T GRCh37
NC_000012.10:g.7836946A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.285A>T MANE Select ENSP00000229307.4:p.Lys95Asn
ENST00000229307.8:c.285A>T ENSP00000229307.4:p.Lys95Asn
ENST00000526286.1:c.285A>T ENSP00000435288.1:p.Lys95Asn
ENST00000526434.2:n.429A>T
ENST00000541267.5:c.213A>T ENSP00000444434.1:p.Lys71Asn
NM_001297698.1:c.285A>T NP_001284627.1:p.Lys95Asn
NM_024865.3:c.285A>T NP_079141.2:p.Lys95Asn
XM_011520850.1:c.285A>T XP_011519152.1:p.Lys95Asn
XM_011520851.1:c.213A>T XP_011519153.1:p.Lys71Asn
XM_011520852.1:c.-88A>T XP_011519154.1:n.-88A>T
NM_024865.4:c.285A>T MANE Select NP_079141.2:p.Lys95Asn
NM_001297698.2:c.285A>T NP_001284627.1:p.Lys95Asn