Canonical Allele Identifier: CA2843608662

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679511_186679512insTAAG , CM000663.2:g.186679511_186679512insTAAG	GRCh38
NC_000001.10:g.186648643_186648644insTAAG , CM000663.1:g.186648643_186648644insTAAG	GRCh37
NC_000001.9:g.184915266_184915267insTAAG	NCBI36
NG_028206.2:g.5916_5917insCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.53-74_53-73insCTTA MANE Select	ENSP00000356438.5:n.53-74_53-73insCTTA
ENST00000680451.1:c.53-74_53-73insCTTA	ENSP00000506242.1:n.53-74_53-73insCTTA
ENST00000681605.1:c.53-74_53-73insCTTA	ENSP00000504900.1:n.53-74_53-73insCTTA
ENST00000367468.9:c.53-74_53-73insCTTA	ENSP00000356438.5:n.53-74_53-73insCTTA
ENST00000490885.6:n.186-74_186-73insCTTA
ENST00000559627.1:c.53-74_53-73insCTTA	ENSP00000454130.1:n.53-74_53-73insCTTA
ENST00000559800.1:n.186-74_186-73insCTTA
NM_000963.3:c.53-74_53-73insCTTA	NP_000954.1:n.53-74_53-73insCTTA
NM_000963.4:c.53-74_53-73insCTTA MANE Select	NP_000954.1:n.53-74_53-73insCTTA