Canonical Allele Identifier: CA2631005611

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510355-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510355A>G , CM000678.2:g.1510355A>G	GRCh38
NC_000016.9:g.1560356A>G , CM000678.1:g.1560356A>G	GRCh37
NC_000016.8:g.1500357A>G	NCBI36
NG_032783.1:g.106754T>C
NG_050910.1:g.22012A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*419A>G MANE Select	ENSP00000262319.6:n.*419A>G
ENST00000262319.10:c.*419A>G	ENSP00000262319.6:n.*419A>G
ENST00000568240.1:n.1225A>G
NM_016111.3:c.*419A>G	NP_057195.2:n.*419A>G
XM_011522773.1:c.*419A>G	XP_011521075.1:n.*419A>G
XM_011522774.1:c.*419A>G	XP_011521076.1:n.*419A>G
XM_011522775.1:c.*419A>G	XP_011521077.1:n.*419A>G
XM_011522776.1:c.*419A>G	XP_011521078.1:n.*419A>G
XR_932982.1:n.3232A>G
NM_001351846.1:c.*419A>G	NP_001338775.1:n.*419A>G
XM_011522773.3:c.*419A>G	XP_011521075.1:n.*419A>G
XM_011522774.2:c.*419A>G	XP_011521076.1:n.*419A>G
XM_011522775.3:c.*419A>G	XP_011521077.1:n.*419A>G
XM_011522776.2:c.*419A>G	XP_011521078.1:n.*419A>G
XR_001752042.2:n.3465A>G
XR_001752043.2:n.2980A>G
XR_001752044.2:n.2917A>G
XR_932982.3:n.3010A>G
NM_016111.4:c.*419A>G MANE Select	NP_057195.2:n.*419A>G
NM_001351846.2:c.*419A>G	NP_001338775.1:n.*419A>G