Canonical Allele Identifier: CA10581580
Gene: TELO2 HGNC NCBI

Linked Data

dbSNP Id: rs878853273
gnomAD v4: 16-1505602-G-A
MyVariant Identifiers: chr16:g.1555603G>A (hg19) chr16:g.1505602G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1505602G>A , CM000678.2:g.1505602G>A GRCh38
NC_000016.9:g.1555603G>A , CM000678.1:g.1555603G>A GRCh37
NC_000016.8:g.1495604G>A NCBI36
NG_050910.1:g.17259G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262319.11:c.2034+1G>A MANE Select ENSP00000262319.6:n.2034+1G>A
ENST00000262319.10:c.2034+1G>A ENSP00000262319.6:n.2034+1G>A
ENST00000497339.6:c.1228-671G>A ENSP00000456383.1:n.1228-671G>A
ENST00000563676.1:n.161+1G>A
ENST00000564507.5:n.629+1G>A
ENST00000567423.1:c.454+1G>A
ENST00000567427.1:n.233+1G>A
ENST00000569744.1:n.463+1G>A
NM_016111.3:c.2034+1G>A NP_057195.2:n.2034+1G>A
XM_006720993.2:c.2034+1G>A XP_006721056.1:n.2034+1G>A
XM_011522773.1:c.2034+1G>A XP_011521075.1:n.2034+1G>A
XM_011522774.1:c.2034+1G>A XP_011521076.1:n.2034+1G>A
XM_011522775.1:c.2034+1G>A XP_011521077.1:n.2034+1G>A
XM_011522776.1:c.2034+1G>A XP_011521078.1:n.2034+1G>A
XM_011522777.1:c.2034+1G>A XP_011521079.1:n.2034+1G>A
XM_011522778.1:c.2034+1G>A XP_011521080.1:n.2034+1G>A
XR_932982.1:n.2320+1G>A
NM_001351846.1:c.2034+1G>A NP_001338775.1:n.2034+1G>A
XM_011522773.3:c.2034+1G>A XP_011521075.1:n.2034+1G>A
XM_011522774.2:c.2034+1G>A XP_011521076.1:n.2034+1G>A
XM_011522775.3:c.2034+1G>A XP_011521077.1:n.2034+1G>A
XM_011522776.2:c.2034+1G>A XP_011521078.1:n.2034+1G>A
XM_011522777.3:c.2034+1G>A XP_011521079.1:n.2034+1G>A
XM_011522778.3:c.2034+1G>A XP_011521080.1:n.2034+1G>A
XR_001752042.2:n.2098+1G>A
XR_001752043.2:n.2081+1G>A
XR_001752044.2:n.2018+1G>A
XR_932982.3:n.2098+1G>A
NM_016111.4:c.2034+1G>A MANE Select NP_057195.2:n.2034+1G>A
NM_001351846.2:c.2034+1G>A NP_001338775.1:n.2034+1G>A
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