Canonical Allele Identifier: CA2201717954

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510274T= , CM000678.2:g.1510274T=	GRCh38
NC_000016.9:g.1560275T= , CM000678.1:g.1560275T=	GRCh37
NC_000016.8:g.1500276T=	NCBI36
NG_032783.1:g.106835A=
NG_050910.1:g.21931T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*338T= MANE Select	ENSP00000262319.6:n.*338T=
ENST00000262319.10:c.*338T=	ENSP00000262319.6:n.*338T=
ENST00000568240.1:n.1144T=
NM_016111.3:c.*338T=	NP_057195.2:n.*338T=
XM_011522773.1:c.*338T=	XP_011521075.1:n.*338T=
XM_011522774.1:c.*338T=	XP_011521076.1:n.*338T=
XM_011522775.1:c.*338T=	XP_011521077.1:n.*338T=
XM_011522776.1:c.*338T=	XP_011521078.1:n.*338T=
XR_932982.1:n.3151T=
NM_001351846.1:c.*338T=	NP_001338775.1:n.*338T=
XM_011522773.3:c.*338T=	XP_011521075.1:n.*338T=
XM_011522774.2:c.*338T=	XP_011521076.1:n.*338T=
XM_011522775.3:c.*338T=	XP_011521077.1:n.*338T=
XM_011522776.2:c.*338T=	XP_011521078.1:n.*338T=
XR_001752042.2:n.3384T=
XR_001752043.2:n.2899T=
XR_001752044.2:n.2836T=
XR_932982.3:n.2929T=
NM_016111.4:c.*338T= MANE Select	NP_057195.2:n.*338T=
NM_001351846.2:c.*338T=	NP_001338775.1:n.*338T=