Canonical Allele Identifier: CA374780607

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122381434-T-C
• MyVariant Identifiers: chr9:g.125143713T>C (hg19) ; chr9:g.122381434T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381434T>C , CM000671.2:g.122381434T>C	GRCh38
NC_000009.11:g.125143713T>C , CM000671.1:g.125143713T>C	GRCh37
NC_000009.10:g.124183534T>C	NCBI36
NG_032900.1:g.15485T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.560T>C MANE Select	ENSP00000354612.2:p.Ile187Thr
ENST00000373698.7:c.233T>C	ENSP00000362802.5:p.Ile78Thr
ENST00000426608.6:c.313-62T>C	ENSP00000411606.2:n.313-62T>C
ENST00000540753.6:c.485T>C	ENSP00000437709.1:p.Ile162Thr
ENST00000619306.5:c.416T>C	ENSP00000483540.2:p.Ile139Thr
ENST00000643576.1:n.654T>C
ENST00000643810.1:c.233T>C	ENSP00000494717.1:p.Ile78Thr
ENST00000645132.1:n.519+2861T>C
ENST00000647067.1:c.*405T>C	ENSP00000495728.1:n.*405T>C
ENST00000223423.8:c.560T>C	ENSP00000223423.4:p.Ile187Thr
ENST00000362012.6:c.560T>C	ENSP00000354612.2:p.Ile187Thr
ENST00000373698.6:c.233T>C	ENSP00000362802.5:p.Ile78Thr
ENST00000426608.5:c.304-62T>C	ENSP00000411606.1:n.304-62T>C
ENST00000540753.5:c.485T>C	ENSP00000437709.1:p.Ile162Thr
ENST00000614910.4:c.416T>C	ENSP00000484800.1:p.Ile139Thr
ENST00000619306.4:c.653T>C	ENSP00000483540.1:p.Ile218Thr
NM_000962.3:c.560T>C	NP_000953.2:p.Ile187Thr
NM_001271164.1:c.416T>C	NP_001258093.1:p.Ile139Thr
NM_001271165.1:c.233T>C	NP_001258094.1:p.Ile78Thr
NM_001271166.1:c.233T>C	NP_001258095.1:p.Ile78Thr
NM_001271367.1:c.233T>C	NP_001258296.1:p.Ile78Thr
NM_001271368.1:c.485T>C	NP_001258297.1:p.Ile162Thr
NM_080591.2:c.560T>C	NP_542158.1:p.Ile187Thr
XM_005252105.2:c.485T>C	XP_005252162.1:p.Ile162Thr
XM_011518875.1:c.485T>C	XP_011517177.1:p.Ile162Thr
XM_011518876.1:c.233T>C	XP_011517178.1:p.Ile78Thr
XM_005252105.3:c.485T>C	XP_005252162.1:p.Ile162Thr
XM_011518875.2:c.485T>C	XP_011517177.1:p.Ile162Thr
XM_011518876.2:c.233T>C	XP_011517178.1:p.Ile78Thr
XM_024447614.1:c.233T>C	XP_024303382.1:p.Ile78Thr
XM_024447615.1:c.233T>C	XP_024303383.1:p.Ile78Thr
NM_000962.4:c.560T>C MANE Select	NP_000953.2:p.Ile187Thr
NM_001271164.2:c.416T>C	NP_001258093.1:p.Ile139Thr
NM_001271165.2:c.233T>C	NP_001258094.1:p.Ile78Thr
NM_001271166.2:c.233T>C	NP_001258095.1:p.Ile78Thr
NM_001271367.2:c.233T>C	NP_001258296.1:p.Ile78Thr
NM_001271368.2:c.485T>C	NP_001258297.1:p.Ile162Thr
NM_080591.3:c.560T>C	NP_542158.1:p.Ile187Thr