Canonical Allele Identifier: CA2201718050

Gene: TELO2

Linked Data

• dbSNP Id: rs887850972
• gnomAD v4: 16-1510417-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510417G>A , CM000678.2:g.1510417G>A	GRCh38
NC_000016.9:g.1560418G>A , CM000678.1:g.1560418G>A	GRCh37
NC_000016.8:g.1500419G>A	NCBI36
NG_032783.1:g.106692C>T
NG_050910.1:g.22074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*481G>A MANE Select	ENSP00000262319.6:n.*481G>A
ENST00000262319.10:c.*481G>A	ENSP00000262319.6:n.*481G>A
ENST00000568240.1:n.1287G>A
NM_016111.3:c.*481G>A	NP_057195.2:n.*481G>A
XM_011522773.1:c.*481G>A	XP_011521075.1:n.*481G>A
XM_011522774.1:c.*481G>A	XP_011521076.1:n.*481G>A
XM_011522775.1:c.*481G>A	XP_011521077.1:n.*481G>A
XM_011522776.1:c.*481G>A	XP_011521078.1:n.*481G>A
XR_932982.1:n.3294G>A
NM_001351846.1:c.*481G>A	NP_001338775.1:n.*481G>A
XM_011522773.3:c.*481G>A	XP_011521075.1:n.*481G>A
XM_011522774.2:c.*481G>A	XP_011521076.1:n.*481G>A
XM_011522775.3:c.*481G>A	XP_011521077.1:n.*481G>A
XM_011522776.2:c.*481G>A	XP_011521078.1:n.*481G>A
XR_001752042.2:n.3527G>A
XR_001752043.2:n.3042G>A
XR_001752044.2:n.2979G>A
XR_932982.3:n.3072G>A
NM_016111.4:c.*481G>A MANE Select	NP_057195.2:n.*481G>A
NM_001351846.2:c.*481G>A	NP_001338775.1:n.*481G>A