Canonical Allele Identifier: CA859724472

Gene: PTGS1

Linked Data

• dbSNP Id: rs1274375428
• MyVariant Identifiers: chr9:g.125135403del (hg19) ; chr9:g.122373124del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122373126del , CM000671.2:g.122373126del	GRCh38
NC_000009.11:g.125135405del , CM000671.1:g.125135405del	GRCh37
NC_000009.10:g.124175226del	NCBI36
NG_032900.1:g.7177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.94+1854del MANE Select	ENSP00000354612.2:n.94+1854del
ENST00000426608.6:c.94+1854del	ENSP00000411606.2:n.94+1854del
ENST00000540753.6:c.19+1292del	ENSP00000437709.1:n.19+1292del
ENST00000619306.5:c.94+1854del	ENSP00000483540.2:n.94+1854del
ENST00000643576.1:n.188+1854del
ENST00000643810.1:c.-234+1854del	ENSP00000494717.1:n.-234+1854del
ENST00000645132.1:n.261+1854del
ENST00000647067.1:c.94+1854del	ENSP00000495728.1:n.94+1854del
ENST00000223423.8:c.94+1854del	ENSP00000223423.4:n.94+1854del
ENST00000362012.6:c.94+1854del	ENSP00000354612.2:n.94+1854del
ENST00000426608.5:c.85+1854del	ENSP00000411606.1:n.85+1854del
ENST00000540753.5:c.19+1292del	ENSP00000437709.1:n.19+1292del
ENST00000614910.4:c.94+1854del	ENSP00000484800.1:n.94+1854del
ENST00000619306.4:c.187+1854del	ENSP00000483540.1:n.187+1854del
NM_000962.3:c.94+1854del	NP_000953.2:n.94+1854del
NM_001271164.1:c.94+1854del	NP_001258093.1:n.94+1854del
NM_001271166.1:c.-234+1854del	NP_001258095.1:n.-234+1854del
NM_001271367.1:c.-205+1854del	NP_001258296.1:n.-205+1854del
NM_001271368.1:c.19+1292del	NP_001258297.1:n.19+1292del
NM_080591.2:c.94+1854del	NP_542158.1:n.94+1854del
XM_005252105.2:c.19+1292del	XP_005252162.1:n.19+1292del
XM_011518875.1:c.19+1292del	XP_011517177.1:n.19+1292del
XM_011518876.1:c.-2552del	XP_011517178.1:n.-2552del
XM_005252105.3:c.19+1292del	XP_005252162.1:n.19+1292del
XM_011518875.2:c.19+1292del	XP_011517177.1:n.19+1292del
XM_011518876.2:c.-2552del	XP_011517178.1:n.-2552del
XM_024447614.1:c.-234+1854del	XP_024303382.1:n.-234+1854del
XM_024447615.1:c.-234+1854del	XP_024303383.1:n.-234+1854del
NM_000962.4:c.94+1854del MANE Select	NP_000953.2:n.94+1854del
NM_001271164.2:c.94+1854del	NP_001258093.1:n.94+1854del
NM_001271166.2:c.-234+1854del	NP_001258095.1:n.-234+1854del
NM_001271367.2:c.-205+1854del	NP_001258296.1:n.-205+1854del
NM_001271368.2:c.19+1292del	NP_001258297.1:n.19+1292del
NM_080591.3:c.94+1854del	NP_542158.1:n.94+1854del