Canonical Allele Identifier: CA2631005305

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510129-CTGGGCACTGCCCGCCGGGACATGGCAGCCTGGACGTGGGGCTGGGGCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510135_1510183del , CM000678.2:g.1510135_1510183del	GRCh38
NC_000016.9:g.1560136_1560184del , CM000678.1:g.1560136_1560184del	GRCh37
NC_000016.8:g.1500137_1500185del	NCBI36
NG_032783.1:g.106931_106979del
NG_050910.1:g.21792_21840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*199_*247del MANE Select	ENSP00000262319.6:n.*199_*247del
ENST00000262319.10:c.*199_*247del	ENSP00000262319.6:n.*199_*247del
ENST00000568240.1:n.1005_1053del
NM_016111.3:c.*199_*247del	NP_057195.2:n.*199_*247del
XM_011522773.1:c.*199_*247del	XP_011521075.1:n.*199_*247del
XM_011522774.1:c.*199_*247del	XP_011521076.1:n.*199_*247del
XM_011522775.1:c.*199_*247del	XP_011521077.1:n.*199_*247del
XM_011522776.1:c.*199_*247del	XP_011521078.1:n.*199_*247del
XR_932982.1:n.3012_3060del
NM_001351846.1:c.*199_*247del	NP_001338775.1:n.*199_*247del
XM_011522773.3:c.*199_*247del	XP_011521075.1:n.*199_*247del
XM_011522774.2:c.*199_*247del	XP_011521076.1:n.*199_*247del
XM_011522775.3:c.*199_*247del	XP_011521077.1:n.*199_*247del
XM_011522776.2:c.*199_*247del	XP_011521078.1:n.*199_*247del
XR_001752042.2:n.3245_3293del
XR_001752043.2:n.2760_2808del
XR_001752044.2:n.2697_2745del
XR_932982.3:n.2790_2838del
NM_016111.4:c.*199_*247del MANE Select	NP_057195.2:n.*199_*247del
NM_001351846.2:c.*199_*247del	NP_001338775.1:n.*199_*247del