Canonical Allele Identifier: CA2805557593
Gene: TELO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510282G>A , CM000678.2:g.1510282G>A GRCh38
NC_000016.9:g.1560283G>A , CM000678.1:g.1560283G>A GRCh37
NC_000016.8:g.1500284G>A NCBI36
NG_032783.1:g.106827C>T
NG_050910.1:g.21939G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*346G>A MANE Select ENSP00000262319.6:n.*346G>A
ENST00000262319.10:c.*346G>A ENSP00000262319.6:n.*346G>A
ENST00000568240.1:n.1152G>A
NM_016111.3:c.*346G>A NP_057195.2:n.*346G>A
XM_011522773.1:c.*346G>A XP_011521075.1:n.*346G>A
XM_011522774.1:c.*346G>A XP_011521076.1:n.*346G>A
XM_011522775.1:c.*346G>A XP_011521077.1:n.*346G>A
XM_011522776.1:c.*346G>A XP_011521078.1:n.*346G>A
XR_932982.1:n.3159G>A
NM_001351846.1:c.*346G>A NP_001338775.1:n.*346G>A
XM_011522773.3:c.*346G>A XP_011521075.1:n.*346G>A
XM_011522774.2:c.*346G>A XP_011521076.1:n.*346G>A
XM_011522775.3:c.*346G>A XP_011521077.1:n.*346G>A
XM_011522776.2:c.*346G>A XP_011521078.1:n.*346G>A
XR_001752042.2:n.3392G>A
XR_001752043.2:n.2907G>A
XR_001752044.2:n.2844G>A
XR_932982.3:n.2937G>A
NM_016111.4:c.*346G>A MANE Select NP_057195.2:n.*346G>A
NM_001351846.2:c.*346G>A NP_001338775.1:n.*346G>A