Canonical Allele Identifier: CA492927962

Gene: TELO2

Linked Data

• MyVariant Identifiers: chr16:g.1555515C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1505514C>G , CM000678.2:g.1505514C>G	GRCh38
NC_000016.9:g.1555515C>G , CM000678.1:g.1555515C>G	GRCh37
NC_000016.8:g.1495516C>G	NCBI36
NG_050910.1:g.17171C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.1947C>G MANE Select	ENSP00000262319.6:p.Ala649=
ENST00000262319.10:c.1947C>G	ENSP00000262319.6:p.Ala649=
ENST00000497339.6:c.1228-759C>G	ENSP00000456383.1:n.1228-759C>G
ENST00000563676.1:n.74C>G
ENST00000564507.5:n.542C>G
ENST00000567423.1:c.367C>G
ENST00000567427.1:n.146C>G
ENST00000569744.1:n.376C>G
NM_016111.3:c.1947C>G	NP_057195.2:p.Ala649=
XM_006720993.2:c.1947C>G	XP_006721056.1:p.Ala649=
XM_011522773.1:c.1947C>G	XP_011521075.1:p.Ala649=
XM_011522774.1:c.1947C>G	XP_011521076.1:p.Ala649=
XM_011522775.1:c.1947C>G	XP_011521077.1:p.Ala649=
XM_011522776.1:c.1947C>G	XP_011521078.1:p.Ala649=
XM_011522777.1:c.1947C>G	XP_011521079.1:p.Ala649=
XM_011522778.1:c.1947C>G	XP_011521080.1:p.Ala649=
XR_932982.1:n.2233C>G
XR_932983.1:n.2153C>G
NM_001351846.1:c.1947C>G	NP_001338775.1:p.Ala649=
XM_011522773.3:c.1947C>G	XP_011521075.1:p.Ala649=
XM_011522774.2:c.1947C>G	XP_011521076.1:p.Ala649=
XM_011522775.3:c.1947C>G	XP_011521077.1:p.Ala649=
XM_011522776.2:c.1947C>G	XP_011521078.1:p.Ala649=
XM_011522777.3:c.1947C>G	XP_011521079.1:p.Ala649=
XM_011522778.3:c.1947C>G	XP_011521080.1:p.Ala649=
XR_001752042.2:n.2011C>G
XR_001752043.2:n.1994C>G
XR_001752044.2:n.1931C>G
XR_932982.3:n.2011C>G
NM_016111.4:c.1947C>G MANE Select	NP_057195.2:p.Ala649=
NM_001351846.2:c.1947C>G	NP_001338775.1:p.Ala649=