Canonical Allele Identifier: CA2631005011
Gene: TELO2 HGNC NCBI

Linked Data

gnomAD v4: 16-1505290-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1505290A>G , CM000678.2:g.1505290A>G GRCh38
NC_000016.9:g.1555291A>G , CM000678.1:g.1555291A>G GRCh37
NC_000016.8:g.1495292A>G NCBI36
NG_050910.1:g.16947A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.1843-120A>G MANE Select ENSP00000262319.6:n.1843-120A>G
ENST00000262319.10:c.1843-120A>G ENSP00000262319.6:n.1843-120A>G
ENST00000497339.6:c.1228-983A>G ENSP00000456383.1:n.1228-983A>G
ENST00000564507.5:n.438-120A>G
ENST00000567423.1:c.263-120A>G
ENST00000567427.1:n.42-120A>G
ENST00000569744.1:n.152A>G
NM_016111.3:c.1843-120A>G NP_057195.2:n.1843-120A>G
XM_006720993.2:c.1843-120A>G XP_006721056.1:n.1843-120A>G
XM_011522773.1:c.1843-120A>G XP_011521075.1:n.1843-120A>G
XM_011522774.1:c.1843-120A>G XP_011521076.1:n.1843-120A>G
XM_011522775.1:c.1843-120A>G XP_011521077.1:n.1843-120A>G
XM_011522776.1:c.1843-120A>G XP_011521078.1:n.1843-120A>G
XM_011522777.1:c.1843-120A>G XP_011521079.1:n.1843-120A>G
XM_011522778.1:c.1843-120A>G XP_011521080.1:n.1843-120A>G
XR_932982.1:n.2129-120A>G
XR_932983.1:n.2049-120A>G
NM_001351846.1:c.1843-120A>G NP_001338775.1:n.1843-120A>G
XM_011522773.3:c.1843-120A>G XP_011521075.1:n.1843-120A>G
XM_011522774.2:c.1843-120A>G XP_011521076.1:n.1843-120A>G
XM_011522775.3:c.1843-120A>G XP_011521077.1:n.1843-120A>G
XM_011522776.2:c.1843-120A>G XP_011521078.1:n.1843-120A>G
XM_011522777.3:c.1843-120A>G XP_011521079.1:n.1843-120A>G
XM_011522778.3:c.1843-120A>G XP_011521080.1:n.1843-120A>G
XR_001752042.2:n.1907-120A>G
XR_001752043.2:n.1890-120A>G
XR_001752044.2:n.1827-120A>G
XR_932982.3:n.1907-120A>G
NM_016111.4:c.1843-120A>G MANE Select NP_057195.2:n.1843-120A>G
NM_001351846.2:c.1843-120A>G NP_001338775.1:n.1843-120A>G