Canonical Allele Identifier: CA2201717872
Gene: TELO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510217A= , CM000678.2:g.1510217A= GRCh38
NC_000016.9:g.1560218A= , CM000678.1:g.1560218A= GRCh37
NC_000016.8:g.1500219A= NCBI36
NG_032783.1:g.106892T=
NG_050910.1:g.21874A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*281A= MANE Select ENSP00000262319.6:n.*281A=
ENST00000262319.10:c.*281A= ENSP00000262319.6:n.*281A=
ENST00000568240.1:n.1087A=
NM_016111.3:c.*281A= NP_057195.2:n.*281A=
XM_011522773.1:c.*281A= XP_011521075.1:n.*281A=
XM_011522774.1:c.*281A= XP_011521076.1:n.*281A=
XM_011522775.1:c.*281A= XP_011521077.1:n.*281A=
XM_011522776.1:c.*281A= XP_011521078.1:n.*281A=
XR_932982.1:n.3094A=
NM_001351846.1:c.*281A= NP_001338775.1:n.*281A=
XM_011522773.3:c.*281A= XP_011521075.1:n.*281A=
XM_011522774.2:c.*281A= XP_011521076.1:n.*281A=
XM_011522775.3:c.*281A= XP_011521077.1:n.*281A=
XM_011522776.2:c.*281A= XP_011521078.1:n.*281A=
XR_001752042.2:n.3327A=
XR_001752043.2:n.2842A=
XR_001752044.2:n.2779A=
XR_932982.3:n.2872A=
NM_016111.4:c.*281A= MANE Select NP_057195.2:n.*281A=
NM_001351846.2:c.*281A= NP_001338775.1:n.*281A=