Canonical Allele Identifier: CA1213245303
Gene: PTGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679581_186679582delinsGC , CM000663.2:g.186679581_186679582delinsGC GRCh38
NC_000001.10:g.186648713_186648714delinsGC , CM000663.1:g.186648713_186648714delinsGC GRCh37
NC_000001.9:g.184915336_184915337delinsGC NCBI36
NG_028206.2:g.5846_5847delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-144_53-143delinsGC MANE Select ENSP00000356438.5:n.53-144_53-143delinsGC...
ENST00000680451.1:c.53-144_53-143delinsGC ENSP00000506242.1:n.53-144_53-143delinsGC...
ENST00000681605.1:c.53-144_53-143delinsGC ENSP00000504900.1:n.53-144_53-143delinsGC...
ENST00000367468.9:c.53-144_53-143delinsGC ENSP00000356438.5:n.53-144_53-143delinsGC...
ENST00000490885.6:n.186-144_186-143delinsGC
ENST00000559627.1:c.53-144_53-143delinsGC ENSP00000454130.1:n.53-144_53-143delinsGC...
ENST00000559800.1:n.186-144_186-143delinsGC
NM_000963.3:c.53-144_53-143delinsGC NP_000954.1:n.53-144_53-143delinsGC
NM_000963.4:c.53-144_53-143delinsGC MANE Select NP_000954.1:n.53-144_53-143delinsGC
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