Canonical Allele Identifier: CA2631005037
Gene: TELO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1505310del , CM000678.2:g.1505310del GRCh38
NC_000016.9:g.1555311del , CM000678.1:g.1555311del GRCh37
NC_000016.8:g.1495312del NCBI36
NG_050910.1:g.16967del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.1843-100del MANE Select ENSP00000262319.6:n.1843-100del
ENST00000262319.10:c.1843-100del ENSP00000262319.6:n.1843-100del
ENST00000497339.6:c.1228-963del ENSP00000456383.1:n.1228-963del
ENST00000564507.5:n.438-100del
ENST00000567423.1:c.263-100del
ENST00000567427.1:n.42-100del
ENST00000569744.1:n.172del
NM_016111.3:c.1843-100del NP_057195.2:n.1843-100del
XM_006720993.2:c.1843-100del XP_006721056.1:n.1843-100del
XM_011522773.1:c.1843-100del XP_011521075.1:n.1843-100del
XM_011522774.1:c.1843-100del XP_011521076.1:n.1843-100del
XM_011522775.1:c.1843-100del XP_011521077.1:n.1843-100del
XM_011522776.1:c.1843-100del XP_011521078.1:n.1843-100del
XM_011522777.1:c.1843-100del XP_011521079.1:n.1843-100del
XM_011522778.1:c.1843-100del XP_011521080.1:n.1843-100del
XR_932982.1:n.2129-100del
XR_932983.1:n.2049-100del
NM_001351846.1:c.1843-100del NP_001338775.1:n.1843-100del
XM_011522773.3:c.1843-100del XP_011521075.1:n.1843-100del
XM_011522774.2:c.1843-100del XP_011521076.1:n.1843-100del
XM_011522775.3:c.1843-100del XP_011521077.1:n.1843-100del
XM_011522776.2:c.1843-100del XP_011521078.1:n.1843-100del
XM_011522777.3:c.1843-100del XP_011521079.1:n.1843-100del
XM_011522778.3:c.1843-100del XP_011521080.1:n.1843-100del
XR_001752042.2:n.1907-100del
XR_001752043.2:n.1890-100del
XR_001752044.2:n.1827-100del
XR_932982.3:n.1907-100del
NM_016111.4:c.1843-100del MANE Select NP_057195.2:n.1843-100del
NM_001351846.2:c.1843-100del NP_001338775.1:n.1843-100del