Canonical Allele Identifier: CA276667805

Gene: TELO2

Linked Data

• dbSNP Id: rs972330149
• gnomAD v4: 16-1510346-CAGG-C
• MyVariant Identifiers: chr16:g.1560348_1560350del (hg19) ; chr16:g.1510347_1510349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510349_1510351del , CM000678.2:g.1510349_1510351del	GRCh38
NC_000016.9:g.1560350_1560352del , CM000678.1:g.1560350_1560352del	GRCh37
NC_000016.8:g.1500351_1500353del	NCBI36
NG_032783.1:g.106760_106762del
NG_050910.1:g.22006_22008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*413_*415del MANE Select	ENSP00000262319.6:n.*413_*415del
ENST00000262319.10:c.*413_*415del	ENSP00000262319.6:n.*413_*415del
ENST00000568240.1:n.1219_1221del
NM_016111.3:c.*413_*415del	NP_057195.2:n.*413_*415del
XM_011522773.1:c.*413_*415del	XP_011521075.1:n.*413_*415del
XM_011522774.1:c.*413_*415del	XP_011521076.1:n.*413_*415del
XM_011522775.1:c.*413_*415del	XP_011521077.1:n.*413_*415del
XM_011522776.1:c.*413_*415del	XP_011521078.1:n.*413_*415del
XR_932982.1:n.3226_3228del
NM_001351846.1:c.*413_*415del	NP_001338775.1:n.*413_*415del
XM_011522773.3:c.*413_*415del	XP_011521075.1:n.*413_*415del
XM_011522774.2:c.*413_*415del	XP_011521076.1:n.*413_*415del
XM_011522775.3:c.*413_*415del	XP_011521077.1:n.*413_*415del
XM_011522776.2:c.*413_*415del	XP_011521078.1:n.*413_*415del
XR_001752042.2:n.3459_3461del
XR_001752043.2:n.2974_2976del
XR_001752044.2:n.2911_2913del
XR_932982.3:n.3004_3006del
NM_016111.4:c.*413_*415del MANE Select	NP_057195.2:n.*413_*415del
NM_001351846.2:c.*413_*415del	NP_001338775.1:n.*413_*415del