Canonical Allele Identifier: CA2631005426

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510203-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510205del , CM000678.2:g.1510205del	GRCh38
NC_000016.9:g.1560206del , CM000678.1:g.1560206del	GRCh37
NC_000016.8:g.1500207del	NCBI36
NG_032783.1:g.106905del
NG_050910.1:g.21862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*269del MANE Select	ENSP00000262319.6:n.*269del
ENST00000262319.10:c.*269del	ENSP00000262319.6:n.*269del
ENST00000568240.1:n.1075del
NM_016111.3:c.*269del	NP_057195.2:n.*269del
XM_011522773.1:c.*269del	XP_011521075.1:n.*269del
XM_011522774.1:c.*269del	XP_011521076.1:n.*269del
XM_011522775.1:c.*269del	XP_011521077.1:n.*269del
XM_011522776.1:c.*269del	XP_011521078.1:n.*269del
XR_932982.1:n.3082del
NM_001351846.1:c.*269del	NP_001338775.1:n.*269del
XM_011522773.3:c.*269del	XP_011521075.1:n.*269del
XM_011522774.2:c.*269del	XP_011521076.1:n.*269del
XM_011522775.3:c.*269del	XP_011521077.1:n.*269del
XM_011522776.2:c.*269del	XP_011521078.1:n.*269del
XR_001752042.2:n.3315del
XR_001752043.2:n.2830del
XR_001752044.2:n.2767del
XR_932982.3:n.2860del
NM_016111.4:c.*269del MANE Select	NP_057195.2:n.*269del
NM_001351846.2:c.*269del	NP_001338775.1:n.*269del