Canonical Allele Identifier: CA2574102012
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679524del , CM000663.2:g.186679524del GRCh38
NC_000001.10:g.186648656del , CM000663.1:g.186648656del GRCh37
NC_000001.9:g.184915279del NCBI36
NG_028206.2:g.5906del

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-84del MANE Select ENSP00000356438.5:n.53-84del
ENST00000680451.1:c.53-84del ENSP00000506242.1:n.53-84del
ENST00000681605.1:c.53-84del ENSP00000504900.1:n.53-84del
ENST00000367468.9:c.53-84del ENSP00000356438.5:n.53-84del
ENST00000490885.6:n.186-84del
ENST00000559627.1:c.53-84del ENSP00000454130.1:n.53-84del
ENST00000559800.1:n.186-84del
NM_000963.3:c.53-84del NP_000954.1:n.53-84del
NM_000963.4:c.53-84del MANE Select NP_000954.1:n.53-84del