Canonical Allele Identifier: CA2201718014

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510327G= , CM000678.2:g.1510327G=	GRCh38
NC_000016.9:g.1560328G= , CM000678.1:g.1560328G=	GRCh37
NC_000016.8:g.1500329G=	NCBI36
NG_032783.1:g.106782C=
NG_050910.1:g.21984G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*391G= MANE Select	ENSP00000262319.6:n.*391G=
ENST00000262319.10:c.*391G=	ENSP00000262319.6:n.*391G=
ENST00000568240.1:n.1197G=
NM_016111.3:c.*391G=	NP_057195.2:n.*391G=
XM_011522773.1:c.*391G=	XP_011521075.1:n.*391G=
XM_011522774.1:c.*391G=	XP_011521076.1:n.*391G=
XM_011522775.1:c.*391G=	XP_011521077.1:n.*391G=
XM_011522776.1:c.*391G=	XP_011521078.1:n.*391G=
XR_932982.1:n.3204G=
NM_001351846.1:c.*391G=	NP_001338775.1:n.*391G=
XM_011522773.3:c.*391G=	XP_011521075.1:n.*391G=
XM_011522774.2:c.*391G=	XP_011521076.1:n.*391G=
XM_011522775.3:c.*391G=	XP_011521077.1:n.*391G=
XM_011522776.2:c.*391G=	XP_011521078.1:n.*391G=
XR_001752042.2:n.3437G=
XR_001752043.2:n.2952G=
XR_001752044.2:n.2889G=
XR_932982.3:n.2982G=
NM_016111.4:c.*391G= MANE Select	NP_057195.2:n.*391G=
NM_001351846.2:c.*391G=	NP_001338775.1:n.*391G=