Canonical Allele Identifier: CA2201709473
Gene: TELO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1505391_1505392delinsTG , CM000678.2:g.1505391_1505392delinsTG GRCh38
NC_000016.9:g.1555392_1555393delinsTG , CM000678.1:g.1555392_1555393delinsTG GRCh37
NC_000016.8:g.1495393_1495394delinsTG NCBI36
NG_050910.1:g.17048_17049delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.1843-19_1843-18delinsTG MANE Select ENSP00000262319.6:n.1843-19_1843-18delinsTG
ENST00000262319.10:c.1843-19_1843-18delinsTG ENSP00000262319.6:n.1843-19_1843-18delinsTG
ENST00000497339.6:c.1228-882_1228-881delinsTG ENSP00000456383.1:n.1228-882_1228-881delinsTG
ENST00000564507.5:n.438-19_438-18delinsTG
ENST00000567423.1:c.263-19_263-18delinsTG
ENST00000567427.1:n.42-19_42-18delinsTG
ENST00000569744.1:n.253_254delinsTG
NM_016111.3:c.1843-19_1843-18delinsTG NP_057195.2:n.1843-19_1843-18delinsTG
XM_006720993.2:c.1843-19_1843-18delinsTG XP_006721056.1:n.1843-19_1843-18delinsTG
XM_011522773.1:c.1843-19_1843-18delinsTG XP_011521075.1:n.1843-19_1843-18delinsTG
XM_011522774.1:c.1843-19_1843-18delinsTG XP_011521076.1:n.1843-19_1843-18delinsTG
XM_011522775.1:c.1843-19_1843-18delinsTG XP_011521077.1:n.1843-19_1843-18delinsTG
XM_011522776.1:c.1843-19_1843-18delinsTG XP_011521078.1:n.1843-19_1843-18delinsTG
XM_011522777.1:c.1843-19_1843-18delinsTG XP_011521079.1:n.1843-19_1843-18delinsTG
XM_011522778.1:c.1843-19_1843-18delinsTG XP_011521080.1:n.1843-19_1843-18delinsTG
XR_932982.1:n.2129-19_2129-18delinsTG
XR_932983.1:n.2049-19_2049-18delinsTG
NM_001351846.1:c.1843-19_1843-18delinsTG NP_001338775.1:n.1843-19_1843-18delinsTG
XM_011522773.3:c.1843-19_1843-18delinsTG XP_011521075.1:n.1843-19_1843-18delinsTG
XM_011522774.2:c.1843-19_1843-18delinsTG XP_011521076.1:n.1843-19_1843-18delinsTG
XM_011522775.3:c.1843-19_1843-18delinsTG XP_011521077.1:n.1843-19_1843-18delinsTG
XM_011522776.2:c.1843-19_1843-18delinsTG XP_011521078.1:n.1843-19_1843-18delinsTG
XM_011522777.3:c.1843-19_1843-18delinsTG XP_011521079.1:n.1843-19_1843-18delinsTG
XM_011522778.3:c.1843-19_1843-18delinsTG XP_011521080.1:n.1843-19_1843-18delinsTG
XR_001752042.2:n.1907-19_1907-18delinsTG
XR_001752043.2:n.1890-19_1890-18delinsTG
XR_001752044.2:n.1827-19_1827-18delinsTG
XR_932982.3:n.1907-19_1907-18delinsTG
NM_016111.4:c.1843-19_1843-18delinsTG MANE Select NP_057195.2:n.1843-19_1843-18delinsTG
NM_001351846.2:c.1843-19_1843-18delinsTG NP_001338775.1:n.1843-19_1843-18delinsTG