Canonical Allele Identifier: CA1213245635

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680372_186680375delinsTGAG , CM000663.2:g.186680372_186680375delinsTGAG	GRCh38
NC_000001.10:g.186649504_186649507delinsTGAG , CM000663.1:g.186649504_186649507delinsTGAG	GRCh37
NC_000001.9:g.184916127_184916130delinsTGAG	NCBI36
NG_028206.2:g.5053_5056delinsCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-85_-82delinsCTCA MANE Select	ENSP00000356438.5:n.-85_-82delinsCTCA
ENST00000680451.1:c.-85_-82delinsCTCA	ENSP00000506242.1:n.-85_-82delinsCTCA
ENST00000681605.1:c.-85_-82delinsCTCA	ENSP00000504900.1:n.-85_-82delinsCTCA
ENST00000367468.9:c.-85_-82delinsCTCA	ENSP00000356438.5:n.-85_-82delinsCTCA
ENST00000490885.6:n.49_52delinsCTCA
ENST00000559800.1:n.49_52delinsCTCA
NM_000963.3:c.-85_-82delinsCTCA	NP_000954.1:n.-85_-82delinsCTCA
NM_000963.4:c.-85_-82delinsCTCA MANE Select	NP_000954.1:n.-85_-82delinsCTCA