Canonical Allele Identifier: CA2201717995

Gene: TELO2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510305C= , CM000678.2:g.1510305C=	GRCh38
NC_000016.9:g.1560306C= , CM000678.1:g.1560306C=	GRCh37
NC_000016.8:g.1500307C=	NCBI36
NG_032783.1:g.106804G=
NG_050910.1:g.21962C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*369C= MANE Select	ENSP00000262319.6:n.*369C=
ENST00000262319.10:c.*369C=	ENSP00000262319.6:n.*369C=
ENST00000568240.1:n.1175C=
NM_016111.3:c.*369C=	NP_057195.2:n.*369C=
XM_011522773.1:c.*369C=	XP_011521075.1:n.*369C=
XM_011522774.1:c.*369C=	XP_011521076.1:n.*369C=
XM_011522775.1:c.*369C=	XP_011521077.1:n.*369C=
XM_011522776.1:c.*369C=	XP_011521078.1:n.*369C=
XR_932982.1:n.3182C=
NM_001351846.1:c.*369C=	NP_001338775.1:n.*369C=
XM_011522773.3:c.*369C=	XP_011521075.1:n.*369C=
XM_011522774.2:c.*369C=	XP_011521076.1:n.*369C=
XM_011522775.3:c.*369C=	XP_011521077.1:n.*369C=
XM_011522776.2:c.*369C=	XP_011521078.1:n.*369C=
XR_001752042.2:n.3415C=
XR_001752043.2:n.2930C=
XR_001752044.2:n.2867C=
XR_932982.3:n.2960C=
NM_016111.4:c.*369C= MANE Select	NP_057195.2:n.*369C=
NM_001351846.2:c.*369C=	NP_001338775.1:n.*369C=