Canonical Allele Identifier: CA2631005520
Gene: TELO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510279_1510281del , CM000678.2:g.1510279_1510281del GRCh38
NC_000016.9:g.1560280_1560282del , CM000678.1:g.1560280_1560282del GRCh37
NC_000016.8:g.1500281_1500283del NCBI36
NG_032783.1:g.106828_106830del
NG_050910.1:g.21936_21938del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*343_*345del MANE Select ENSP00000262319.6:n.*343_*345del
ENST00000262319.10:c.*343_*345del ENSP00000262319.6:n.*343_*345del
ENST00000568240.1:n.1149_1151del
NM_016111.3:c.*343_*345del NP_057195.2:n.*343_*345del
XM_011522773.1:c.*343_*345del XP_011521075.1:n.*343_*345del
XM_011522774.1:c.*343_*345del XP_011521076.1:n.*343_*345del
XM_011522775.1:c.*343_*345del XP_011521077.1:n.*343_*345del
XM_011522776.1:c.*343_*345del XP_011521078.1:n.*343_*345del
XR_932982.1:n.3156_3158del
NM_001351846.1:c.*343_*345del NP_001338775.1:n.*343_*345del
XM_011522773.3:c.*343_*345del XP_011521075.1:n.*343_*345del
XM_011522774.2:c.*343_*345del XP_011521076.1:n.*343_*345del
XM_011522775.3:c.*343_*345del XP_011521077.1:n.*343_*345del
XM_011522776.2:c.*343_*345del XP_011521078.1:n.*343_*345del
XR_001752042.2:n.3389_3391del
XR_001752043.2:n.2904_2906del
XR_001752044.2:n.2841_2843del
XR_932982.3:n.2934_2936del
NM_016111.4:c.*343_*345del MANE Select NP_057195.2:n.*343_*345del
NM_001351846.2:c.*343_*345del NP_001338775.1:n.*343_*345del