Canonical Allele Identifier: CA2805557597

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510317_1510318del , CM000678.2:g.1510317_1510318del	GRCh38
NC_000016.9:g.1560318_1560319del , CM000678.1:g.1560318_1560319del	GRCh37
NC_000016.8:g.1500319_1500320del	NCBI36
NG_032783.1:g.106791_106792del
NG_050910.1:g.21974_21975del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*381_*382del MANE Select	ENSP00000262319.6:n.*381_*382del
ENST00000262319.10:c.*381_*382del	ENSP00000262319.6:n.*381_*382del
ENST00000568240.1:n.1187_1188del
NM_016111.3:c.*381_*382del	NP_057195.2:n.*381_*382del
XM_011522773.1:c.*381_*382del	XP_011521075.1:n.*381_*382del
XM_011522774.1:c.*381_*382del	XP_011521076.1:n.*381_*382del
XM_011522775.1:c.*381_*382del	XP_011521077.1:n.*381_*382del
XM_011522776.1:c.*381_*382del	XP_011521078.1:n.*381_*382del
XR_932982.1:n.3194_3195del
NM_001351846.1:c.*381_*382del	NP_001338775.1:n.*381_*382del
XM_011522773.3:c.*381_*382del	XP_011521075.1:n.*381_*382del
XM_011522774.2:c.*381_*382del	XP_011521076.1:n.*381_*382del
XM_011522775.3:c.*381_*382del	XP_011521077.1:n.*381_*382del
XM_011522776.2:c.*381_*382del	XP_011521078.1:n.*381_*382del
XR_001752042.2:n.3427_3428del
XR_001752043.2:n.2942_2943del
XR_001752044.2:n.2879_2880del
XR_932982.3:n.2972_2973del
NM_016111.4:c.*381_*382del MANE Select	NP_057195.2:n.*381_*382del
NM_001351846.2:c.*381_*382del	NP_001338775.1:n.*381_*382del