Canonical Allele Identifier: CA2631005579

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510326-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510326_1510327insAG , CM000678.2:g.1510326_1510327insAG	GRCh38
NC_000016.9:g.1560327_1560328insAG , CM000678.1:g.1560327_1560328insAG	GRCh37
NC_000016.8:g.1500328_1500329insAG	NCBI36
NG_032783.1:g.106782_106783insCT
NG_050910.1:g.21983_21984insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*390_*391insAG MANE Select	ENSP00000262319.6:n.*390_*391insAG
ENST00000262319.10:c.*390_*391insAG	ENSP00000262319.6:n.*390_*391insAG
ENST00000568240.1:n.1196_1197insAG
NM_016111.3:c.*390_*391insAG	NP_057195.2:n.*390_*391insAG
XM_011522773.1:c.*390_*391insAG	XP_011521075.1:n.*390_*391insAG
XM_011522774.1:c.*390_*391insAG	XP_011521076.1:n.*390_*391insAG
XM_011522775.1:c.*390_*391insAG	XP_011521077.1:n.*390_*391insAG
XM_011522776.1:c.*390_*391insAG	XP_011521078.1:n.*390_*391insAG
XR_932982.1:n.3203_3204insAG
NM_001351846.1:c.*390_*391insAG	NP_001338775.1:n.*390_*391insAG
XM_011522773.3:c.*390_*391insAG	XP_011521075.1:n.*390_*391insAG
XM_011522774.2:c.*390_*391insAG	XP_011521076.1:n.*390_*391insAG
XM_011522775.3:c.*390_*391insAG	XP_011521077.1:n.*390_*391insAG
XM_011522776.2:c.*390_*391insAG	XP_011521078.1:n.*390_*391insAG
XR_001752042.2:n.3436_3437insAG
XR_001752043.2:n.2951_2952insAG
XR_001752044.2:n.2888_2889insAG
XR_932982.3:n.2981_2982insAG
NM_016111.4:c.*390_*391insAG MANE Select	NP_057195.2:n.*390_*391insAG
NM_001351846.2:c.*390_*391insAG	NP_001338775.1:n.*390_*391insAG