Canonical Allele Identifier: CA728762987

Gene: PTGS2

Linked Data

• dbSNP Id: rs1445816165
• MyVariant Identifiers: chr1:g.186648643_186648667del (hg19) ; chr1:g.186679511_186679535del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679512_186679536del , CM000663.2:g.186679512_186679536del	GRCh38
NC_000001.10:g.186648644_186648668del , CM000663.1:g.186648644_186648668del	GRCh37
NC_000001.9:g.184915267_184915291del	NCBI36
NG_028206.2:g.5893_5917del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.53-97_53-73del MANE Select	ENSP00000356438.5:n.53-97_53-73del
ENST00000680451.1:c.53-97_53-73del	ENSP00000506242.1:n.53-97_53-73del
ENST00000681605.1:c.53-97_53-73del	ENSP00000504900.1:n.53-97_53-73del
ENST00000367468.9:c.53-97_53-73del	ENSP00000356438.5:n.53-97_53-73del
ENST00000490885.6:n.186-97_186-73del
ENST00000559627.1:c.53-97_53-73del	ENSP00000454130.1:n.53-97_53-73del
ENST00000559800.1:n.186-97_186-73del
NM_000963.3:c.53-97_53-73del	NP_000954.1:n.53-97_53-73del
NM_000963.4:c.53-97_53-73del MANE Select	NP_000954.1:n.53-97_53-73del