Canonical Allele Identifier: CA2691550290

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122371131-CCTCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371132_122371136del , CM000671.2:g.122371132_122371136del	GRCh38
NC_000009.11:g.125133411_125133415del , CM000671.1:g.125133411_125133415del	GRCh37
NC_000009.10:g.124173232_124173236del	NCBI36
NG_032900.1:g.5183_5187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.7+41_7+45del MANE Select	ENSP00000354612.2:n.7+41_7+45del
ENST00000426608.6:c.7+41_7+45del	ENSP00000411606.2:n.7+41_7+45del
ENST00000540753.6:c.-290-54_-290-50del	ENSP00000437709.1:n.-290-54_-290-50del
ENST00000619306.5:c.7+41_7+45del	ENSP00000483540.2:n.7+41_7+45del
ENST00000643576.1:n.48_52del
ENST00000643810.1:c.-320-54_-320-50del	ENSP00000494717.1:n.-320-54_-320-50del
ENST00000645132.1:n.121_125del
ENST00000647067.1:c.7+41_7+45del	ENSP00000495728.1:n.7+41_7+45del
ENST00000223423.8:c.7+41_7+45del	ENSP00000223423.4:n.7+41_7+45del
ENST00000362012.6:c.7+41_7+45del	ENSP00000354612.2:n.7+41_7+45del
ENST00000540753.5:c.-290-54_-290-50del	ENSP00000437709.1:n.-290-54_-290-50del
ENST00000614910.4:c.7+41_7+45del	ENSP00000484800.1:n.7+41_7+45del
ENST00000619306.4:c.48_52del	ENSP00000483540.1:p.Ser17ValfsTer4
NM_000962.3:c.7+41_7+45del	NP_000953.2:n.7+41_7+45del
NM_001271164.1:c.7+41_7+45del	NP_001258093.1:n.7+41_7+45del
NM_001271166.1:c.-320-54_-320-50del	NP_001258095.1:n.-320-54_-320-50del
NM_001271367.1:c.-292+41_-292+45del	NP_001258296.1:n.-292+41_-292+45del
NM_001271368.1:c.-290-54_-290-50del	NP_001258297.1:n.-290-54_-290-50del
NM_080591.2:c.7+41_7+45del	NP_542158.1:n.7+41_7+45del
XM_005252105.2:c.-291+41_-291+45del	XP_005252162.1:n.-291+41_-291+45del
XM_011518875.1:c.-290-54_-290-50del	XP_011517177.1:n.-290-54_-290-50del
XM_011518876.1:c.-4152-54_-4152-50del	XP_011517178.1:n.-4152-54_-4152-50del
XM_005252105.3:c.-291+41_-291+45del	XP_005252162.1:n.-291+41_-291+45del
XM_011518875.2:c.-290-54_-290-50del	XP_011517177.1:n.-290-54_-290-50del
XM_011518876.2:c.-4152-54_-4152-50del	XP_011517178.1:n.-4152-54_-4152-50del
XM_024447614.1:c.-320-54_-320-50del	XP_024303382.1:n.-320-54_-320-50del
XM_024447615.1:c.-320-54_-320-50del	XP_024303383.1:n.-320-54_-320-50del
NM_000962.4:c.7+41_7+45del MANE Select	NP_000953.2:n.7+41_7+45del
NM_001271164.2:c.7+41_7+45del	NP_001258093.1:n.7+41_7+45del
NM_001271166.2:c.-320-54_-320-50del	NP_001258095.1:n.-320-54_-320-50del
NM_001271367.2:c.-292+41_-292+45del	NP_001258296.1:n.-292+41_-292+45del
NM_001271368.2:c.-290-54_-290-50del	NP_001258297.1:n.-290-54_-290-50del
NM_080591.3:c.7+41_7+45del	NP_542158.1:n.7+41_7+45del