Canonical Allele Identifier: CA620343044

Gene: TELO2

Linked Data

• dbSNP Id: rs1459987284
• gnomAD v2: 16-1560263-A-AGCC
• gnomAD v3: 16-1510262-A-AGCC
• gnomAD v4: 16-1510262-A-AGCC
• MyVariant Identifiers: chr16:g.1560263_1560264insGCC (hg19) ; chr16:g.1510262_1510263insGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510263_1510265dup , CM000678.2:g.1510263_1510265dup	GRCh38
NC_000016.9:g.1560264_1560266dup , CM000678.1:g.1560264_1560266dup	GRCh37
NC_000016.8:g.1500265_1500267dup	NCBI36
NG_032783.1:g.106844_106846dup
NG_050910.1:g.21920_21922dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*327_*329dup MANE Select	ENSP00000262319.6:n.*327_*329dup
ENST00000262319.10:c.*327_*329dup	ENSP00000262319.6:n.*327_*329dup
ENST00000568240.1:n.1133_1135dup
NM_016111.3:c.*327_*329dup	NP_057195.2:n.*327_*329dup
XM_011522773.1:c.*327_*329dup	XP_011521075.1:n.*327_*329dup
XM_011522774.1:c.*327_*329dup	XP_011521076.1:n.*327_*329dup
XM_011522775.1:c.*327_*329dup	XP_011521077.1:n.*327_*329dup
XM_011522776.1:c.*327_*329dup	XP_011521078.1:n.*327_*329dup
XR_932982.1:n.3140_3142dup
NM_001351846.1:c.*327_*329dup	NP_001338775.1:n.*327_*329dup
XM_011522773.3:c.*327_*329dup	XP_011521075.1:n.*327_*329dup
XM_011522774.2:c.*327_*329dup	XP_011521076.1:n.*327_*329dup
XM_011522775.3:c.*327_*329dup	XP_011521077.1:n.*327_*329dup
XM_011522776.2:c.*327_*329dup	XP_011521078.1:n.*327_*329dup
XR_001752042.2:n.3373_3375dup
XR_001752043.2:n.2888_2890dup
XR_001752044.2:n.2825_2827dup
XR_932982.3:n.2918_2920dup
NM_016111.4:c.*327_*329dup MANE Select	NP_057195.2:n.*327_*329dup
NM_001351846.2:c.*327_*329dup	NP_001338775.1:n.*327_*329dup