Canonical Allele Identifier: CA1877490250

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370810_122370811delinsTG , CM000671.2:g.122370810_122370811delinsTG	GRCh38
NC_000009.11:g.125133089_125133090delinsTG , CM000671.1:g.125133089_125133090delinsTG	GRCh37
NC_000009.10:g.124172910_124172911delinsTG	NCBI36
NG_032900.1:g.4861_4862delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-323_-322delinsTG	ENSP00000437709.1:n.-323_-322delinsTG
ENST00000643810.1:c.-353_-352delinsTG	ENSP00000494717.1:n.-353_-352delinsTG
ENST00000540753.5:c.-323_-322delinsTG	ENSP00000437709.1:n.-323_-322delinsTG
NM_001271166.1:c.-353_-352delinsTG	NP_001258095.1:n.-353_-352delinsTG
NM_001271368.1:c.-323_-322delinsTG	NP_001258297.1:n.-323_-322delinsTG
XM_011518875.1:c.-323_-322delinsTG	XP_011517177.1:n.-323_-322delinsTG
XM_011518876.1:c.-4185_-4184delinsTG	XP_011517178.1:n.-4185_-4184delinsTG
XM_011518875.2:c.-323_-322delinsTG	XP_011517177.1:n.-323_-322delinsTG
XM_011518876.2:c.-4185_-4184delinsTG	XP_011517178.1:n.-4185_-4184delinsTG
XM_024447614.1:c.-353_-352delinsTG	XP_024303382.1:n.-353_-352delinsTG
XM_024447615.1:c.-353_-352delinsTG	XP_024303383.1:n.-353_-352delinsTG
NM_001271166.2:c.-353_-352delinsTG	NP_001258095.1:n.-353_-352delinsTG
NM_001271368.2:c.-323_-322delinsTG	NP_001258297.1:n.-323_-322delinsTG