Canonical Allele Identifier: CA2617437546
Gene: NANOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793214_7793217del , CM000674.2:g.7793214_7793217del GRCh38
NC_000012.11:g.7945810_7945813del , CM000674.1:g.7945810_7945813del GRCh37
NC_000012.10:g.7837077_7837080del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.414+2_414+5del
ENST00000229307.8:c.414+2_414+5del
ENST00000526286.1:c.414+2_414+5del
ENST00000541267.5:c.342+2_342+5del
NM_001297698.1:c.414+2_414+5del
NM_024865.3:c.414+2_414+5del
XM_011520850.1:c.414+2_414+5del
XM_011520851.1:c.342+2_342+5del
XM_011520852.1:c.42+2_42+5del
NM_024865.4:c.414+2_414+5del
NM_001297698.2:c.414+2_414+5del