Canonical Allele Identifier: CA2631005557

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510308-CTCTTGTCCCAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510311_1510322del , CM000678.2:g.1510311_1510322del	GRCh38
NC_000016.9:g.1560312_1560323del , CM000678.1:g.1560312_1560323del	GRCh37
NC_000016.8:g.1500313_1500324del	NCBI36
NG_032783.1:g.106789_106800del
NG_050910.1:g.21968_21979del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*375_*386del MANE Select	ENSP00000262319.6:n.*375_*386del
ENST00000262319.10:c.*375_*386del	ENSP00000262319.6:n.*375_*386del
ENST00000568240.1:n.1181_1192del
NM_016111.3:c.*375_*386del	NP_057195.2:n.*375_*386del
XM_011522773.1:c.*375_*386del	XP_011521075.1:n.*375_*386del
XM_011522774.1:c.*375_*386del	XP_011521076.1:n.*375_*386del
XM_011522775.1:c.*375_*386del	XP_011521077.1:n.*375_*386del
XM_011522776.1:c.*375_*386del	XP_011521078.1:n.*375_*386del
XR_932982.1:n.3188_3199del
NM_001351846.1:c.*375_*386del	NP_001338775.1:n.*375_*386del
XM_011522773.3:c.*375_*386del	XP_011521075.1:n.*375_*386del
XM_011522774.2:c.*375_*386del	XP_011521076.1:n.*375_*386del
XM_011522775.3:c.*375_*386del	XP_011521077.1:n.*375_*386del
XM_011522776.2:c.*375_*386del	XP_011521078.1:n.*375_*386del
XR_001752042.2:n.3421_3432del
XR_001752043.2:n.2936_2947del
XR_001752044.2:n.2873_2884del
XR_932982.3:n.2966_2977del
NM_016111.4:c.*375_*386del MANE Select	NP_057195.2:n.*375_*386del
NM_001351846.2:c.*375_*386del	NP_001338775.1:n.*375_*386del