Canonical Allele Identifier: CA2631005396
Gene: TELO2 HGNC NCBI

Linked Data

gnomAD v4: 16-1510185-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510185C>A , CM000678.2:g.1510185C>A GRCh38
NC_000016.9:g.1560186C>A , CM000678.1:g.1560186C>A GRCh37
NC_000016.8:g.1500187C>A NCBI36
NG_032783.1:g.106924G>T
NG_050910.1:g.21842C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*249C>A MANE Select ENSP00000262319.6:n.*249C>A
ENST00000262319.10:c.*249C>A ENSP00000262319.6:n.*249C>A
ENST00000568240.1:n.1055C>A
NM_016111.3:c.*249C>A NP_057195.2:n.*249C>A
XM_011522773.1:c.*249C>A XP_011521075.1:n.*249C>A
XM_011522774.1:c.*249C>A XP_011521076.1:n.*249C>A
XM_011522775.1:c.*249C>A XP_011521077.1:n.*249C>A
XM_011522776.1:c.*249C>A XP_011521078.1:n.*249C>A
XR_932982.1:n.3062C>A
NM_001351846.1:c.*249C>A NP_001338775.1:n.*249C>A
XM_011522773.3:c.*249C>A XP_011521075.1:n.*249C>A
XM_011522774.2:c.*249C>A XP_011521076.1:n.*249C>A
XM_011522775.3:c.*249C>A XP_011521077.1:n.*249C>A
XM_011522776.2:c.*249C>A XP_011521078.1:n.*249C>A
XR_001752042.2:n.3295C>A
XR_001752043.2:n.2810C>A
XR_001752044.2:n.2747C>A
XR_932982.3:n.2840C>A
NM_016111.4:c.*249C>A MANE Select NP_057195.2:n.*249C>A
NM_001351846.2:c.*249C>A NP_001338775.1:n.*249C>A