Canonical Allele Identifier: CA973714884
Gene: TELO2 HGNC NCBI

Linked Data

dbSNP Id: rs2040094401

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510351_1510353del , CM000678.2:g.1510351_1510353del GRCh38
NC_000016.9:g.1560352_1560354del , CM000678.1:g.1560352_1560354del GRCh37
NC_000016.8:g.1500353_1500355del NCBI36
NG_032783.1:g.106757_106759del
NG_050910.1:g.22008_22010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*415_*417del MANE Select ENSP00000262319.6:n.*415_*417del
ENST00000262319.10:c.*415_*417del ENSP00000262319.6:n.*415_*417del
ENST00000568240.1:n.1221_1223del
NM_016111.3:c.*415_*417del NP_057195.2:n.*415_*417del
XM_011522773.1:c.*415_*417del XP_011521075.1:n.*415_*417del
XM_011522774.1:c.*415_*417del XP_011521076.1:n.*415_*417del
XM_011522775.1:c.*415_*417del XP_011521077.1:n.*415_*417del
XM_011522776.1:c.*415_*417del XP_011521078.1:n.*415_*417del
XR_932982.1:n.3228_3230del
NM_001351846.1:c.*415_*417del NP_001338775.1:n.*415_*417del
XM_011522773.3:c.*415_*417del XP_011521075.1:n.*415_*417del
XM_011522774.2:c.*415_*417del XP_011521076.1:n.*415_*417del
XM_011522775.3:c.*415_*417del XP_011521077.1:n.*415_*417del
XM_011522776.2:c.*415_*417del XP_011521078.1:n.*415_*417del
XR_001752042.2:n.3461_3463del
XR_001752043.2:n.2976_2978del
XR_001752044.2:n.2913_2915del
XR_932982.3:n.3006_3008del
NM_016111.4:c.*415_*417del MANE Select NP_057195.2:n.*415_*417del
NM_001351846.2:c.*415_*417del NP_001338775.1:n.*415_*417del