Canonical Allele Identifier: CA2574102030
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680340del , CM000663.2:g.186680340del GRCh38
NC_000001.10:g.186649472del , CM000663.1:g.186649472del GRCh37
NC_000001.9:g.184916095del NCBI36
NG_028206.2:g.5090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-48del MANE Select ENSP00000356438.5:n.-48del
ENST00000680451.1:c.-48del ENSP00000506242.1:n.-48del
ENST00000681605.1:c.-48del ENSP00000504900.1:n.-48del
ENST00000367468.9:c.-48del ENSP00000356438.5:n.-48del
ENST00000490885.6:n.86del
ENST00000559800.1:n.86del
NM_000963.3:c.-48del NP_000954.1:n.-48del
NM_000963.4:c.-48del MANE Select NP_000954.1:n.-48del