Canonical Allele Identifier: CA2201709742

Gene: TELO2

Genomic Alleles

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

Transcript Alleles

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