Canonical Allele Identifier: CA2631005552
Gene: TELO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510306_1510307del , CM000678.2:g.1510306_1510307del GRCh38
NC_000016.9:g.1560307_1560308del , CM000678.1:g.1560307_1560308del GRCh37
NC_000016.8:g.1500308_1500309del NCBI36
NG_032783.1:g.106802_106803del
NG_050910.1:g.21963_21964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*370_*371del MANE Select ENSP00000262319.6:n.*370_*371del
ENST00000262319.10:c.*370_*371del ENSP00000262319.6:n.*370_*371del
ENST00000568240.1:n.1176_1177del
NM_016111.3:c.*370_*371del NP_057195.2:n.*370_*371del
XM_011522773.1:c.*370_*371del XP_011521075.1:n.*370_*371del
XM_011522774.1:c.*370_*371del XP_011521076.1:n.*370_*371del
XM_011522775.1:c.*370_*371del XP_011521077.1:n.*370_*371del
XM_011522776.1:c.*370_*371del XP_011521078.1:n.*370_*371del
XR_932982.1:n.3183_3184del
NM_001351846.1:c.*370_*371del NP_001338775.1:n.*370_*371del
XM_011522773.3:c.*370_*371del XP_011521075.1:n.*370_*371del
XM_011522774.2:c.*370_*371del XP_011521076.1:n.*370_*371del
XM_011522775.3:c.*370_*371del XP_011521077.1:n.*370_*371del
XM_011522776.2:c.*370_*371del XP_011521078.1:n.*370_*371del
XR_001752042.2:n.3416_3417del
XR_001752043.2:n.2931_2932del
XR_001752044.2:n.2868_2869del
XR_932982.3:n.2961_2962del
NM_016111.4:c.*370_*371del MANE Select NP_057195.2:n.*370_*371del
NM_001351846.2:c.*370_*371del NP_001338775.1:n.*370_*371del