Canonical Allele Identifier: CA2631005402

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510188-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510189del , CM000678.2:g.1510189del	GRCh38
NC_000016.9:g.1560190del , CM000678.1:g.1560190del	GRCh37
NC_000016.8:g.1500191del	NCBI36
NG_032783.1:g.106920del
NG_050910.1:g.21846del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*253del MANE Select	ENSP00000262319.6:n.*253del
ENST00000262319.10:c.*253del	ENSP00000262319.6:n.*253del
ENST00000568240.1:n.1059del
NM_016111.3:c.*253del	NP_057195.2:n.*253del
XM_011522773.1:c.*253del	XP_011521075.1:n.*253del
XM_011522774.1:c.*253del	XP_011521076.1:n.*253del
XM_011522775.1:c.*253del	XP_011521077.1:n.*253del
XM_011522776.1:c.*253del	XP_011521078.1:n.*253del
XR_932982.1:n.3066del
NM_001351846.1:c.*253del	NP_001338775.1:n.*253del
XM_011522773.3:c.*253del	XP_011521075.1:n.*253del
XM_011522774.2:c.*253del	XP_011521076.1:n.*253del
XM_011522775.3:c.*253del	XP_011521077.1:n.*253del
XM_011522776.2:c.*253del	XP_011521078.1:n.*253del
XR_001752042.2:n.3299del
XR_001752043.2:n.2814del
XR_001752044.2:n.2751del
XR_932982.3:n.2844del
NM_016111.4:c.*253del MANE Select	NP_057195.2:n.*253del
NM_001351846.2:c.*253del	NP_001338775.1:n.*253del