Canonical Allele Identifier: CA2579443205

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122371048-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371048G>C , CM000671.2:g.122371048G>C	GRCh38
NC_000009.11:g.125133327G>C , CM000671.1:g.125133327G>C	GRCh37
NC_000009.10:g.124173148G>C	NCBI36
NG_032900.1:g.5099G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.-37G>C MANE Select	ENSP00000354612.2:n.-37G>C
ENST00000540753.6:c.-290-138G>C	ENSP00000437709.1:n.-290-138G>C
ENST00000619306.5:c.-37G>C	ENSP00000483540.2:n.-37G>C
ENST00000643810.1:c.-320-138G>C	ENSP00000494717.1:n.-320-138G>C
ENST00000645132.1:n.37G>C
ENST00000647067.1:c.-37G>C	ENSP00000495728.1:n.-37G>C
ENST00000540753.5:c.-290-138G>C	ENSP00000437709.1:n.-290-138G>C
ENST00000614910.4:c.-37G>C	ENSP00000484800.1:n.-37G>C
NM_000962.3:c.-37G>C	NP_000953.2:n.-37G>C
NM_001271164.1:c.-37G>C	NP_001258093.1:n.-37G>C
NM_001271166.1:c.-320-138G>C	NP_001258095.1:n.-320-138G>C
NM_001271367.1:c.-335G>C	NP_001258296.1:n.-335G>C
NM_001271368.1:c.-290-138G>C	NP_001258297.1:n.-290-138G>C
NM_080591.2:c.-37G>C	NP_542158.1:n.-37G>C
XM_011518875.1:c.-290-138G>C	XP_011517177.1:n.-290-138G>C
XM_011518876.1:c.-4152-138G>C	XP_011517178.1:n.-4152-138G>C
XM_011518875.2:c.-290-138G>C	XP_011517177.1:n.-290-138G>C
XM_011518876.2:c.-4152-138G>C	XP_011517178.1:n.-4152-138G>C
XM_024447614.1:c.-320-138G>C	XP_024303382.1:n.-320-138G>C
XM_024447615.1:c.-320-138G>C	XP_024303383.1:n.-320-138G>C
NM_000962.4:c.-37G>C MANE Select	NP_000953.2:n.-37G>C
NM_001271164.2:c.-37G>C	NP_001258093.1:n.-37G>C
NM_001271166.2:c.-320-138G>C	NP_001258095.1:n.-320-138G>C
NM_001271367.2:c.-335G>C	NP_001258296.1:n.-335G>C
NM_001271368.2:c.-290-138G>C	NP_001258297.1:n.-290-138G>C
NM_080591.3:c.-37G>C	NP_542158.1:n.-37G>C