Canonical Allele Identifier: CA1877496544

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381385C= , CM000671.2:g.122381385C=	GRCh38
NC_000009.11:g.125143664C= , CM000671.1:g.125143664C=	GRCh37
NC_000009.10:g.124183485C=	NCBI36
NG_032900.1:g.15436C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.511C= MANE Select	ENSP00000354612.2:p.Pro171=
ENST00000373698.7:c.184C=	ENSP00000362802.5:p.Pro62=
ENST00000426608.6:c.313-111C=	ENSP00000411606.2:n.313-111C=
ENST00000540753.6:c.436C=	ENSP00000437709.1:p.Pro146=
ENST00000619306.5:c.367C=	ENSP00000483540.2:p.Pro123=
ENST00000643576.1:n.605C=
ENST00000643810.1:c.184C=	ENSP00000494717.1:p.Pro62=
ENST00000645132.1:n.519+2812C=
ENST00000647067.1:c.*356C=	ENSP00000495728.1:n.*356C=
ENST00000223423.8:c.511C=	ENSP00000223423.4:p.Pro171=
ENST00000362012.6:c.511C=	ENSP00000354612.2:p.Pro171=
ENST00000373698.6:c.184C=	ENSP00000362802.5:p.Pro62=
ENST00000426608.5:c.304-111C=	ENSP00000411606.1:n.304-111C=
ENST00000540753.5:c.436C=	ENSP00000437709.1:p.Pro146=
ENST00000614910.4:c.367C=	ENSP00000484800.1:p.Pro123=
ENST00000619306.4:c.604C=	ENSP00000483540.1:p.Pro202=
NM_000962.3:c.511C=	NP_000953.2:p.Pro171=
NM_001271164.1:c.367C=	NP_001258093.1:p.Pro123=
NM_001271165.1:c.184C=	NP_001258094.1:p.Pro62=
NM_001271166.1:c.184C=	NP_001258095.1:p.Pro62=
NM_001271367.1:c.184C=	NP_001258296.1:p.Pro62=
NM_001271368.1:c.436C=	NP_001258297.1:p.Pro146=
NM_080591.2:c.511C=	NP_542158.1:p.Pro171=
XM_005252105.2:c.436C=	XP_005252162.1:p.Pro146=
XM_011518875.1:c.436C=	XP_011517177.1:p.Pro146=
XM_011518876.1:c.184C=	XP_011517178.1:p.Pro62=
XM_005252105.3:c.436C=	XP_005252162.1:p.Pro146=
XM_011518875.2:c.436C=	XP_011517177.1:p.Pro146=
XM_011518876.2:c.184C=	XP_011517178.1:p.Pro62=
XM_024447614.1:c.184C=	XP_024303382.1:p.Pro62=
XM_024447615.1:c.184C=	XP_024303383.1:p.Pro62=
NM_000962.4:c.511C= MANE Select	NP_000953.2:p.Pro171=
NM_001271164.2:c.367C=	NP_001258093.1:p.Pro123=
NM_001271165.2:c.184C=	NP_001258094.1:p.Pro62=
NM_001271166.2:c.184C=	NP_001258095.1:p.Pro62=
NM_001271367.2:c.184C=	NP_001258296.1:p.Pro62=
NM_001271368.2:c.436C=	NP_001258297.1:p.Pro146=
NM_080591.3:c.511C=	NP_542158.1:p.Pro171=