Canonical Allele Identifier: CA718375466

Gene: TELO2

Linked Data

• dbSNP Id: rs1337756373
• MyVariant Identifiers: chr16:g.1560281C>G (hg19) ; chr16:g.1510280C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510280C>G , CM000678.2:g.1510280C>G	GRCh38
NC_000016.9:g.1560281C>G , CM000678.1:g.1560281C>G	GRCh37
NC_000016.8:g.1500282C>G	NCBI36
NG_032783.1:g.106829G>C
NG_050910.1:g.21937C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262319.11:c.*344C>G MANE Select	ENSP00000262319.6:n.*344C>G
ENST00000262319.10:c.*344C>G	ENSP00000262319.6:n.*344C>G
ENST00000568240.1:n.1150C>G
NM_016111.3:c.*344C>G	NP_057195.2:n.*344C>G
XM_011522773.1:c.*344C>G	XP_011521075.1:n.*344C>G
XM_011522774.1:c.*344C>G	XP_011521076.1:n.*344C>G
XM_011522775.1:c.*344C>G	XP_011521077.1:n.*344C>G
XM_011522776.1:c.*344C>G	XP_011521078.1:n.*344C>G
XR_932982.1:n.3157C>G
NM_001351846.1:c.*344C>G	NP_001338775.1:n.*344C>G
XM_011522773.3:c.*344C>G	XP_011521075.1:n.*344C>G
XM_011522774.2:c.*344C>G	XP_011521076.1:n.*344C>G
XM_011522775.3:c.*344C>G	XP_011521077.1:n.*344C>G
XM_011522776.2:c.*344C>G	XP_011521078.1:n.*344C>G
XR_001752042.2:n.3390C>G
XR_001752043.2:n.2905C>G
XR_001752044.2:n.2842C>G
XR_932982.3:n.2935C>G
NM_016111.4:c.*344C>G MANE Select	NP_057195.2:n.*344C>G
NM_001351846.2:c.*344C>G	NP_001338775.1:n.*344C>G