Canonical Allele Identifier: CA374780532

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143701G>C (hg19) ; chr9:g.122381422G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381422G>C , CM000671.2:g.122381422G>C	GRCh38
NC_000009.11:g.125143701G>C , CM000671.1:g.125143701G>C	GRCh37
NC_000009.10:g.124183522G>C	NCBI36
NG_032900.1:g.15473G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.548G>C MANE Select	ENSP00000354612.2:p.Arg183Thr
ENST00000373698.7:c.221G>C	ENSP00000362802.5:p.Arg74Thr
ENST00000426608.6:c.313-74G>C	ENSP00000411606.2:n.313-74G>C
ENST00000540753.6:c.473G>C	ENSP00000437709.1:p.Arg158Thr
ENST00000619306.5:c.404G>C	ENSP00000483540.2:p.Arg135Thr
ENST00000643576.1:n.642G>C
ENST00000643810.1:c.221G>C	ENSP00000494717.1:p.Arg74Thr
ENST00000645132.1:n.519+2849G>C
ENST00000647067.1:c.*393G>C	ENSP00000495728.1:n.*393G>C
ENST00000223423.8:c.548G>C	ENSP00000223423.4:p.Arg183Thr
ENST00000362012.6:c.548G>C	ENSP00000354612.2:p.Arg183Thr
ENST00000373698.6:c.221G>C	ENSP00000362802.5:p.Arg74Thr
ENST00000426608.5:c.304-74G>C	ENSP00000411606.1:n.304-74G>C
ENST00000540753.5:c.473G>C	ENSP00000437709.1:p.Arg158Thr
ENST00000614910.4:c.404G>C	ENSP00000484800.1:p.Arg135Thr
ENST00000619306.4:c.641G>C	ENSP00000483540.1:p.Arg214Thr
NM_000962.3:c.548G>C	NP_000953.2:p.Arg183Thr
NM_001271164.1:c.404G>C	NP_001258093.1:p.Arg135Thr
NM_001271165.1:c.221G>C	NP_001258094.1:p.Arg74Thr
NM_001271166.1:c.221G>C	NP_001258095.1:p.Arg74Thr
NM_001271367.1:c.221G>C	NP_001258296.1:p.Arg74Thr
NM_001271368.1:c.473G>C	NP_001258297.1:p.Arg158Thr
NM_080591.2:c.548G>C	NP_542158.1:p.Arg183Thr
XM_005252105.2:c.473G>C	XP_005252162.1:p.Arg158Thr
XM_011518875.1:c.473G>C	XP_011517177.1:p.Arg158Thr
XM_011518876.1:c.221G>C	XP_011517178.1:p.Arg74Thr
XM_005252105.3:c.473G>C	XP_005252162.1:p.Arg158Thr
XM_011518875.2:c.473G>C	XP_011517177.1:p.Arg158Thr
XM_011518876.2:c.221G>C	XP_011517178.1:p.Arg74Thr
XM_024447614.1:c.221G>C	XP_024303382.1:p.Arg74Thr
XM_024447615.1:c.221G>C	XP_024303383.1:p.Arg74Thr
NM_000962.4:c.548G>C MANE Select	NP_000953.2:p.Arg183Thr
NM_001271164.2:c.404G>C	NP_001258093.1:p.Arg135Thr
NM_001271165.2:c.221G>C	NP_001258094.1:p.Arg74Thr
NM_001271166.2:c.221G>C	NP_001258095.1:p.Arg74Thr
NM_001271367.2:c.221G>C	NP_001258296.1:p.Arg74Thr
NM_001271368.2:c.473G>C	NP_001258297.1:p.Arg158Thr
NM_080591.3:c.548G>C	NP_542158.1:p.Arg183Thr