Canonical Allele Identifier: CA2805557583

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510193_1510230del , CM000678.2:g.1510193_1510230del	GRCh38
NC_000016.9:g.1560194_1560231del , CM000678.1:g.1560194_1560231del	GRCh37
NC_000016.8:g.1500195_1500232del	NCBI36
NG_032783.1:g.106885_106922del
NG_050910.1:g.21850_21887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*257_*294del MANE Select	ENSP00000262319.6:n.*257_*294del
ENST00000262319.10:c.*257_*294del	ENSP00000262319.6:n.*257_*294del
ENST00000568240.1:n.1063_1100del
NM_016111.3:c.*257_*294del	NP_057195.2:n.*257_*294del
XM_011522773.1:c.*257_*294del	XP_011521075.1:n.*257_*294del
XM_011522774.1:c.*257_*294del	XP_011521076.1:n.*257_*294del
XM_011522775.1:c.*257_*294del	XP_011521077.1:n.*257_*294del
XM_011522776.1:c.*257_*294del	XP_011521078.1:n.*257_*294del
XR_932982.1:n.3070_3107del
NM_001351846.1:c.*257_*294del	NP_001338775.1:n.*257_*294del
XM_011522773.3:c.*257_*294del	XP_011521075.1:n.*257_*294del
XM_011522774.2:c.*257_*294del	XP_011521076.1:n.*257_*294del
XM_011522775.3:c.*257_*294del	XP_011521077.1:n.*257_*294del
XM_011522776.2:c.*257_*294del	XP_011521078.1:n.*257_*294del
XR_001752042.2:n.3303_3340del
XR_001752043.2:n.2818_2855del
XR_001752044.2:n.2755_2792del
XR_932982.3:n.2848_2885del
NM_016111.4:c.*257_*294del MANE Select	NP_057195.2:n.*257_*294del
NM_001351846.2:c.*257_*294del	NP_001338775.1:n.*257_*294del