Canonical Allele Identifier: CA2509400491

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673767_186673768insCAAATTTATT , CM000663.2:g.186673767_186673768insCAAATTTATT	GRCh38
NC_000001.10:g.186642899_186642900insCAAATTTATT , CM000663.1:g.186642899_186642900insCAAATTTATT	GRCh37
NC_000001.9:g.184909522_184909523insCAAATTTATT	NCBI36
NG_028206.2:g.11660_11661insAATAAATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*585_*586insAATAAATTTG MANE Select	ENSP00000356438.5:n.*585_*586insAATAAATTTG
ENST00000680451.1:c.*585_*586insAATAAATTTG	ENSP00000506242.1:n.*585_*586insAATAAATTTG
ENST00000681605.1:c.*2072_*2073insAATAAATTTG	ENSP00000504900.1:n.*2072_*2073insAATAAATTTG
ENST00000367468.9:c.*585_*586insAATAAATTTG	ENSP00000356438.5:n.*585_*586insAATAAATTTG
ENST00000490885.6:n.2815_2816insAATAAATTTG
NM_000963.3:c.*585_*586insAATAAATTTG	NP_000954.1:n.*585_*586insAATAAATTTG
NM_000963.4:c.*585_*586insAATAAATTTG MANE Select	NP_000954.1:n.*585_*586insAATAAATTTG