Canonical Allele Identifier: CA1213245342

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679694_186679695delinsGT , CM000663.2:g.186679694_186679695delinsGT	GRCh38
NC_000001.10:g.186648826_186648827delinsGT , CM000663.1:g.186648826_186648827delinsGT	GRCh37
NC_000001.9:g.184915449_184915450delinsGT	NCBI36
NG_028206.2:g.5733_5734delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.53-257_53-256delinsAC MANE Select	ENSP00000356438.5:n.53-257_53-256delinsAC
ENST00000680451.1:c.53-257_53-256delinsAC	ENSP00000506242.1:n.53-257_53-256delinsAC
ENST00000681605.1:c.53-257_53-256delinsAC	ENSP00000504900.1:n.53-257_53-256delinsAC
ENST00000367468.9:c.53-257_53-256delinsAC	ENSP00000356438.5:n.53-257_53-256delinsAC
ENST00000490885.6:n.186-257_186-256delinsAC
ENST00000559627.1:c.53-257_53-256delinsAC	ENSP00000454130.1:n.53-257_53-256delinsAC
ENST00000559800.1:n.186-257_186-256delinsAC
NM_000963.3:c.53-257_53-256delinsAC	NP_000954.1:n.53-257_53-256delinsAC
NM_000963.4:c.53-257_53-256delinsAC MANE Select	NP_000954.1:n.53-257_53-256delinsAC