Canonical Allele Identifier: CA1213245413

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679846_186679847delinsCT , CM000663.2:g.186679846_186679847delinsCT	GRCh38
NC_000001.10:g.186648978_186648979delinsCT , CM000663.1:g.186648978_186648979delinsCT	GRCh37
NC_000001.9:g.184915601_184915602delinsCT	NCBI36
NG_028206.2:g.5581_5582delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.52+392_52+393delinsAG MANE Select	ENSP00000356438.5:n.52+392_52+393delinsAG
ENST00000680451.1:c.52+392_52+393delinsAG	ENSP00000506242.1:n.52+392_52+393delinsAG
ENST00000681605.1:c.52+392_52+393delinsAG	ENSP00000504900.1:n.52+392_52+393delinsAG
ENST00000367468.9:c.52+392_52+393delinsAG	ENSP00000356438.5:n.52+392_52+393delinsAG
ENST00000490885.6:n.185+392_185+393delinsAG
ENST00000559627.1:c.52+392_52+393delinsAG	ENSP00000454130.1:n.52+392_52+393delinsAG
ENST00000559800.1:n.185+392_185+393delinsAG
NM_000963.3:c.52+392_52+393delinsAG	NP_000954.1:n.52+392_52+393delinsAG
NM_000963.4:c.52+392_52+393delinsAG MANE Select	NP_000954.1:n.52+392_52+393delinsAG