Canonical Allele Identifier: CA374780541

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143704G>C (hg19) ; chr9:g.122381425G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381425G>C , CM000671.2:g.122381425G>C	GRCh38
NC_000009.11:g.125143704G>C , CM000671.1:g.125143704G>C	GRCh37
NC_000009.10:g.124183525G>C	NCBI36
NG_032900.1:g.15476G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.551G>C MANE Select	ENSP00000354612.2:p.Arg184Thr
ENST00000373698.7:c.224G>C	ENSP00000362802.5:p.Arg75Thr
ENST00000426608.6:c.313-71G>C	ENSP00000411606.2:n.313-71G>C
ENST00000540753.6:c.476G>C	ENSP00000437709.1:p.Arg159Thr
ENST00000619306.5:c.407G>C	ENSP00000483540.2:p.Arg136Thr
ENST00000643576.1:n.645G>C
ENST00000643810.1:c.224G>C	ENSP00000494717.1:p.Arg75Thr
ENST00000645132.1:n.519+2852G>C
ENST00000647067.1:c.*396G>C	ENSP00000495728.1:n.*396G>C
ENST00000223423.8:c.551G>C	ENSP00000223423.4:p.Arg184Thr
ENST00000362012.6:c.551G>C	ENSP00000354612.2:p.Arg184Thr
ENST00000373698.6:c.224G>C	ENSP00000362802.5:p.Arg75Thr
ENST00000426608.5:c.304-71G>C	ENSP00000411606.1:n.304-71G>C
ENST00000540753.5:c.476G>C	ENSP00000437709.1:p.Arg159Thr
ENST00000614910.4:c.407G>C	ENSP00000484800.1:p.Arg136Thr
ENST00000619306.4:c.644G>C	ENSP00000483540.1:p.Arg215Thr
NM_000962.3:c.551G>C	NP_000953.2:p.Arg184Thr
NM_001271164.1:c.407G>C	NP_001258093.1:p.Arg136Thr
NM_001271165.1:c.224G>C	NP_001258094.1:p.Arg75Thr
NM_001271166.1:c.224G>C	NP_001258095.1:p.Arg75Thr
NM_001271367.1:c.224G>C	NP_001258296.1:p.Arg75Thr
NM_001271368.1:c.476G>C	NP_001258297.1:p.Arg159Thr
NM_080591.2:c.551G>C	NP_542158.1:p.Arg184Thr
XM_005252105.2:c.476G>C	XP_005252162.1:p.Arg159Thr
XM_011518875.1:c.476G>C	XP_011517177.1:p.Arg159Thr
XM_011518876.1:c.224G>C	XP_011517178.1:p.Arg75Thr
XM_005252105.3:c.476G>C	XP_005252162.1:p.Arg159Thr
XM_011518875.2:c.476G>C	XP_011517177.1:p.Arg159Thr
XM_011518876.2:c.224G>C	XP_011517178.1:p.Arg75Thr
XM_024447614.1:c.224G>C	XP_024303382.1:p.Arg75Thr
XM_024447615.1:c.224G>C	XP_024303383.1:p.Arg75Thr
NM_000962.4:c.551G>C MANE Select	NP_000953.2:p.Arg184Thr
NM_001271164.2:c.407G>C	NP_001258093.1:p.Arg136Thr
NM_001271165.2:c.224G>C	NP_001258094.1:p.Arg75Thr
NM_001271166.2:c.224G>C	NP_001258095.1:p.Arg75Thr
NM_001271367.2:c.224G>C	NP_001258296.1:p.Arg75Thr
NM_001271368.2:c.476G>C	NP_001258297.1:p.Arg159Thr
NM_080591.3:c.551G>C	NP_542158.1:p.Arg184Thr