Canonical Allele Identifier: CA2201717960

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510278C= , CM000678.2:g.1510278C=	GRCh38
NC_000016.9:g.1560279C= , CM000678.1:g.1560279C=	GRCh37
NC_000016.8:g.1500280C=	NCBI36
NG_032783.1:g.106831G=
NG_050910.1:g.21935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*342C= MANE Select	ENSP00000262319.6:n.*342C=
ENST00000262319.10:c.*342C=	ENSP00000262319.6:n.*342C=
ENST00000568240.1:n.1148C=
NM_016111.3:c.*342C=	NP_057195.2:n.*342C=
XM_011522773.1:c.*342C=	XP_011521075.1:n.*342C=
XM_011522774.1:c.*342C=	XP_011521076.1:n.*342C=
XM_011522775.1:c.*342C=	XP_011521077.1:n.*342C=
XM_011522776.1:c.*342C=	XP_011521078.1:n.*342C=
XR_932982.1:n.3155C=
NM_001351846.1:c.*342C=	NP_001338775.1:n.*342C=
XM_011522773.3:c.*342C=	XP_011521075.1:n.*342C=
XM_011522774.2:c.*342C=	XP_011521076.1:n.*342C=
XM_011522775.3:c.*342C=	XP_011521077.1:n.*342C=
XM_011522776.2:c.*342C=	XP_011521078.1:n.*342C=
XR_001752042.2:n.3388C=
XR_001752043.2:n.2903C=
XR_001752044.2:n.2840C=
XR_932982.3:n.2933C=
NM_016111.4:c.*342C= MANE Select	NP_057195.2:n.*342C=
NM_001351846.2:c.*342C=	NP_001338775.1:n.*342C=