Canonical Allele Identifier: CA2649581801
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186672663-CATT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672673_186672675del , CM000663.2:g.186672673_186672675del GRCh38
NC_000001.10:g.186641805_186641807del , CM000663.1:g.186641805_186641807del GRCh37
NC_000001.9:g.184908428_184908430del NCBI36
NG_028206.2:g.12762_12764del

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1687_*1689del MANE Select ENSP00000356438.5:n.*1687_*1689del
ENST00000680451.1:c.*1687_*1689del ENSP00000506242.1:n.*1687_*1689del
ENST00000681605.1:c.*3174_*3176del ENSP00000504900.1:n.*3174_*3176del
ENST00000367468.9:c.*1687_*1689del ENSP00000356438.5:n.*1687_*1689del
NM_000963.3:c.*1687_*1689del NP_000954.1:n.*1687_*1689del
NM_000963.4:c.*1687_*1689del MANE Select NP_000954.1:n.*1687_*1689del
Search 100 bp 5'
Search 100 bp 3'