Canonical Allele Identifier: CA2746992948
Gene: PTGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673863_186673869del , CM000663.2:g.186673863_186673869del GRCh38
NC_000001.10:g.186642995_186643001del , CM000663.1:g.186642995_186643001del GRCh37
NC_000001.9:g.184909618_184909624del NCBI36
NG_028206.2:g.11563_11569del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*488_*494del MANE Select ENSP00000356438.5:n.*488_*494del
ENST00000680451.1:c.*488_*494del ENSP00000506242.1:n.*488_*494del
ENST00000681605.1:c.*1975_*1981del ENSP00000504900.1:n.*1975_*1981del
ENST00000367468.9:c.*488_*494del ENSP00000356438.5:n.*488_*494del
ENST00000490885.6:n.2718_2724del
NM_000963.3:c.*488_*494del NP_000954.1:n.*488_*494del
NM_000963.4:c.*488_*494del MANE Select NP_000954.1:n.*488_*494del