Canonical Allele Identifier: CA2631005504
Gene: TELO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510268del , CM000678.2:g.1510268del GRCh38
NC_000016.9:g.1560269del , CM000678.1:g.1560269del GRCh37
NC_000016.8:g.1500270del NCBI36
NG_032783.1:g.106845del
NG_050910.1:g.21925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*332del MANE Select ENSP00000262319.6:n.*332del
ENST00000262319.10:c.*332del ENSP00000262319.6:n.*332del
ENST00000568240.1:n.1138del
NM_016111.3:c.*332del NP_057195.2:n.*332del
XM_011522773.1:c.*332del XP_011521075.1:n.*332del
XM_011522774.1:c.*332del XP_011521076.1:n.*332del
XM_011522775.1:c.*332del XP_011521077.1:n.*332del
XM_011522776.1:c.*332del XP_011521078.1:n.*332del
XR_932982.1:n.3145del
NM_001351846.1:c.*332del NP_001338775.1:n.*332del
XM_011522773.3:c.*332del XP_011521075.1:n.*332del
XM_011522774.2:c.*332del XP_011521076.1:n.*332del
XM_011522775.3:c.*332del XP_011521077.1:n.*332del
XM_011522776.2:c.*332del XP_011521078.1:n.*332del
XR_001752042.2:n.3378del
XR_001752043.2:n.2893del
XR_001752044.2:n.2830del
XR_932982.3:n.2923del
NM_016111.4:c.*332del MANE Select NP_057195.2:n.*332del
NM_001351846.2:c.*332del NP_001338775.1:n.*332del