Canonical Allele Identifier: CA276667759

Gene: TELO2

Linked Data

• dbSNP Id: rs976262707
• MyVariant Identifiers: chr16:g.1560273G>C (hg19) ; chr16:g.1510272G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510272G>C , CM000678.2:g.1510272G>C	GRCh38
NC_000016.9:g.1560273G>C , CM000678.1:g.1560273G>C	GRCh37
NC_000016.8:g.1500274G>C	NCBI36
NG_032783.1:g.106837C>G
NG_050910.1:g.21929G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*336G>C MANE Select	ENSP00000262319.6:n.*336G>C
ENST00000262319.10:c.*336G>C	ENSP00000262319.6:n.*336G>C
ENST00000568240.1:n.1142G>C
NM_016111.3:c.*336G>C	NP_057195.2:n.*336G>C
XM_011522773.1:c.*336G>C	XP_011521075.1:n.*336G>C
XM_011522774.1:c.*336G>C	XP_011521076.1:n.*336G>C
XM_011522775.1:c.*336G>C	XP_011521077.1:n.*336G>C
XM_011522776.1:c.*336G>C	XP_011521078.1:n.*336G>C
XR_932982.1:n.3149G>C
NM_001351846.1:c.*336G>C	NP_001338775.1:n.*336G>C
XM_011522773.3:c.*336G>C	XP_011521075.1:n.*336G>C
XM_011522774.2:c.*336G>C	XP_011521076.1:n.*336G>C
XM_011522775.3:c.*336G>C	XP_011521077.1:n.*336G>C
XM_011522776.2:c.*336G>C	XP_011521078.1:n.*336G>C
XR_001752042.2:n.3382G>C
XR_001752043.2:n.2897G>C
XR_001752044.2:n.2834G>C
XR_932982.3:n.2927G>C
NM_016111.4:c.*336G>C MANE Select	NP_057195.2:n.*336G>C
NM_001351846.2:c.*336G>C	NP_001338775.1:n.*336G>C