Canonical Allele Identifier: CA2201717821

Gene: TELO2

Linked Data

• dbSNP Id: rs2040087614

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510174_1510182dup , CM000678.2:g.1510174_1510182dup	GRCh38
NC_000016.9:g.1560175_1560183dup , CM000678.1:g.1560175_1560183dup	GRCh37
NC_000016.8:g.1500176_1500184dup	NCBI36
NG_032783.1:g.106929_106937dup
NG_050910.1:g.21831_21839dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*238_*246dup MANE Select	ENSP00000262319.6:n.*238_*246dup
ENST00000262319.10:c.*238_*246dup	ENSP00000262319.6:n.*238_*246dup
ENST00000568240.1:n.1044_1052dup
NM_016111.3:c.*238_*246dup	NP_057195.2:n.*238_*246dup
XM_011522773.1:c.*238_*246dup	XP_011521075.1:n.*238_*246dup
XM_011522774.1:c.*238_*246dup	XP_011521076.1:n.*238_*246dup
XM_011522775.1:c.*238_*246dup	XP_011521077.1:n.*238_*246dup
XM_011522776.1:c.*238_*246dup	XP_011521078.1:n.*238_*246dup
XR_932982.1:n.3051_3059dup
NM_001351846.1:c.*238_*246dup	NP_001338775.1:n.*238_*246dup
XM_011522773.3:c.*238_*246dup	XP_011521075.1:n.*238_*246dup
XM_011522774.2:c.*238_*246dup	XP_011521076.1:n.*238_*246dup
XM_011522775.3:c.*238_*246dup	XP_011521077.1:n.*238_*246dup
XM_011522776.2:c.*238_*246dup	XP_011521078.1:n.*238_*246dup
XR_001752042.2:n.3284_3292dup
XR_001752043.2:n.2799_2807dup
XR_001752044.2:n.2736_2744dup
XR_932982.3:n.2829_2837dup
NM_016111.4:c.*238_*246dup MANE Select	NP_057195.2:n.*238_*246dup
NM_001351846.2:c.*238_*246dup	NP_001338775.1:n.*238_*246dup