Canonical Allele Identifier: CA1213245275
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679526_186679529delinsCAAT , CM000663.2:g.186679526_186679529delinsCAAT GRCh38
NC_000001.10:g.186648658_186648661delinsCAAT , CM000663.1:g.186648658_186648661delinsCAAT GRCh37
NC_000001.9:g.184915281_184915284delinsCAAT NCBI36
NG_028206.2:g.5899_5902delinsATTG

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-91_53-88delinsATTG MANE Select ENSP00000356438.5:n.53-91_53-88delinsATTG...
ENST00000680451.1:c.53-91_53-88delinsATTG ENSP00000506242.1:n.53-91_53-88delinsATTG...
ENST00000681605.1:c.53-91_53-88delinsATTG ENSP00000504900.1:n.53-91_53-88delinsATTG...
ENST00000367468.9:c.53-91_53-88delinsATTG ENSP00000356438.5:n.53-91_53-88delinsATTG...
ENST00000490885.6:n.186-91_186-88delinsATTG
ENST00000559627.1:c.53-91_53-88delinsATTG ENSP00000454130.1:n.53-91_53-88delinsATTG...
ENST00000559800.1:n.186-91_186-88delinsATTG
NM_000963.3:c.53-91_53-88delinsATTG NP_000954.1:n.53-91_53-88delinsATTG
NM_000963.4:c.53-91_53-88delinsATTG MANE Select NP_000954.1:n.53-91_53-88delinsATTG
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