Canonical Allele Identifier: CA2631005529

Gene: TELO2

Linked Data

• gnomAD v4: 16-1510285-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510285A>C , CM000678.2:g.1510285A>C	GRCh38
NC_000016.9:g.1560286A>C , CM000678.1:g.1560286A>C	GRCh37
NC_000016.8:g.1500287A>C	NCBI36
NG_032783.1:g.106824T>G
NG_050910.1:g.21942A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*349A>C MANE Select	ENSP00000262319.6:n.*349A>C
ENST00000262319.10:c.*349A>C	ENSP00000262319.6:n.*349A>C
ENST00000568240.1:n.1155A>C
NM_016111.3:c.*349A>C	NP_057195.2:n.*349A>C
XM_011522773.1:c.*349A>C	XP_011521075.1:n.*349A>C
XM_011522774.1:c.*349A>C	XP_011521076.1:n.*349A>C
XM_011522775.1:c.*349A>C	XP_011521077.1:n.*349A>C
XM_011522776.1:c.*349A>C	XP_011521078.1:n.*349A>C
XR_932982.1:n.3162A>C
NM_001351846.1:c.*349A>C	NP_001338775.1:n.*349A>C
XM_011522773.3:c.*349A>C	XP_011521075.1:n.*349A>C
XM_011522774.2:c.*349A>C	XP_011521076.1:n.*349A>C
XM_011522775.3:c.*349A>C	XP_011521077.1:n.*349A>C
XM_011522776.2:c.*349A>C	XP_011521078.1:n.*349A>C
XR_001752042.2:n.3395A>C
XR_001752043.2:n.2910A>C
XR_001752044.2:n.2847A>C
XR_932982.3:n.2940A>C
NM_016111.4:c.*349A>C MANE Select	NP_057195.2:n.*349A>C
NM_001351846.2:c.*349A>C	NP_001338775.1:n.*349A>C