Canonical Allele Identifier: CA2201718019

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510346_1510349delinsCAGG , CM000678.2:g.1510346_1510349delinsCAGG	GRCh38
NC_000016.9:g.1560347_1560350delinsCAGG , CM000678.1:g.1560347_1560350delinsCAGG	GRCh37
NC_000016.8:g.1500348_1500351delinsCAGG	NCBI36
NG_032783.1:g.106760_106763delinsCCTG
NG_050910.1:g.22003_22006delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*410_*413delinsCAGG MANE Select	ENSP00000262319.6:n.*410_*413delinsCAGG
ENST00000262319.10:c.*410_*413delinsCAGG	ENSP00000262319.6:n.*410_*413delinsCAGG
ENST00000568240.1:n.1216_1219delinsCAGG
NM_016111.3:c.*410_*413delinsCAGG	NP_057195.2:n.*410_*413delinsCAGG
XM_011522773.1:c.*410_*413delinsCAGG	XP_011521075.1:n.*410_*413delinsCAGG
XM_011522774.1:c.*410_*413delinsCAGG	XP_011521076.1:n.*410_*413delinsCAGG
XM_011522775.1:c.*410_*413delinsCAGG	XP_011521077.1:n.*410_*413delinsCAGG
XM_011522776.1:c.*410_*413delinsCAGG	XP_011521078.1:n.*410_*413delinsCAGG
XR_932982.1:n.3223_3226delinsCAGG
NM_001351846.1:c.*410_*413delinsCAGG	NP_001338775.1:n.*410_*413delinsCAGG
XM_011522773.3:c.*410_*413delinsCAGG	XP_011521075.1:n.*410_*413delinsCAGG
XM_011522774.2:c.*410_*413delinsCAGG	XP_011521076.1:n.*410_*413delinsCAGG
XM_011522775.3:c.*410_*413delinsCAGG	XP_011521077.1:n.*410_*413delinsCAGG
XM_011522776.2:c.*410_*413delinsCAGG	XP_011521078.1:n.*410_*413delinsCAGG
XR_001752042.2:n.3456_3459delinsCAGG
XR_001752043.2:n.2971_2974delinsCAGG
XR_001752044.2:n.2908_2911delinsCAGG
XR_932982.3:n.3001_3004delinsCAGG
NM_016111.4:c.*410_*413delinsCAGG MANE Select	NP_057195.2:n.*410_*413delinsCAGG
NM_001351846.2:c.*410_*413delinsCAGG	NP_001338775.1:n.*410_*413delinsCAGG