Canonical Allele Identifier: CA2631005429

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510204-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510204T>A , CM000678.2:g.1510204T>A	GRCh38
NC_000016.9:g.1560205T>A , CM000678.1:g.1560205T>A	GRCh37
NC_000016.8:g.1500206T>A	NCBI36
NG_032783.1:g.106905A>T
NG_050910.1:g.21861T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*268T>A MANE Select	ENSP00000262319.6:n.*268T>A
ENST00000262319.10:c.*268T>A	ENSP00000262319.6:n.*268T>A
ENST00000568240.1:n.1074T>A
NM_016111.3:c.*268T>A	NP_057195.2:n.*268T>A
XM_011522773.1:c.*268T>A	XP_011521075.1:n.*268T>A
XM_011522774.1:c.*268T>A	XP_011521076.1:n.*268T>A
XM_011522775.1:c.*268T>A	XP_011521077.1:n.*268T>A
XM_011522776.1:c.*268T>A	XP_011521078.1:n.*268T>A
XR_932982.1:n.3081T>A
NM_001351846.1:c.*268T>A	NP_001338775.1:n.*268T>A
XM_011522773.3:c.*268T>A	XP_011521075.1:n.*268T>A
XM_011522774.2:c.*268T>A	XP_011521076.1:n.*268T>A
XM_011522775.3:c.*268T>A	XP_011521077.1:n.*268T>A
XM_011522776.2:c.*268T>A	XP_011521078.1:n.*268T>A
XR_001752042.2:n.3314T>A
XR_001752043.2:n.2829T>A
XR_001752044.2:n.2766T>A
XR_932982.3:n.2859T>A
NM_016111.4:c.*268T>A MANE Select	NP_057195.2:n.*268T>A
NM_001351846.2:c.*268T>A	NP_001338775.1:n.*268T>A