Canonical Allele Identifier: CA2691551907

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122381396-GCTCCTGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381398_122381406del , CM000671.2:g.122381398_122381406del	GRCh38
NC_000009.11:g.125143677_125143685del , CM000671.1:g.125143677_125143685del	GRCh37
NC_000009.10:g.124183498_124183506del	NCBI36
NG_032900.1:g.15449_15457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.524_532del MANE Select	ENSP00000354612.2:p.Leu175_Ala177del
ENST00000373698.7:c.197_205del	ENSP00000362802.5:p.Leu66_Ala68del
ENST00000426608.6:c.313-98_313-90del	ENSP00000411606.2:n.313-98_313-90del
ENST00000540753.6:c.449_457del	ENSP00000437709.1:p.Leu150_Ala152del
ENST00000619306.5:c.380_388del	ENSP00000483540.2:p.Leu127_Ala129del
ENST00000643576.1:n.618_626del
ENST00000643810.1:c.197_205del	ENSP00000494717.1:p.Leu66_Ala68del
ENST00000645132.1:n.519+2825_519+2833del
ENST00000647067.1:c.*369_*377del	ENSP00000495728.1:n.*369_*377del
ENST00000223423.8:c.524_532del	ENSP00000223423.4:p.Leu175_Ala177del
ENST00000362012.6:c.524_532del	ENSP00000354612.2:p.Leu175_Ala177del
ENST00000373698.6:c.197_205del	ENSP00000362802.5:p.Leu66_Ala68del
ENST00000426608.5:c.304-98_304-90del	ENSP00000411606.1:n.304-98_304-90del
ENST00000540753.5:c.449_457del	ENSP00000437709.1:p.Leu150_Ala152del
ENST00000614910.4:c.380_388del	ENSP00000484800.1:p.Leu127_Ala129del
ENST00000619306.4:c.617_625del	ENSP00000483540.1:p.Leu206_Ala208del
NM_000962.3:c.524_532del	NP_000953.2:p.Leu175_Ala177del
NM_001271164.1:c.380_388del	NP_001258093.1:p.Leu127_Ala129del
NM_001271165.1:c.197_205del	NP_001258094.1:p.Leu66_Ala68del
NM_001271166.1:c.197_205del	NP_001258095.1:p.Leu66_Ala68del
NM_001271367.1:c.197_205del	NP_001258296.1:p.Leu66_Ala68del
NM_001271368.1:c.449_457del	NP_001258297.1:p.Leu150_Ala152del
NM_080591.2:c.524_532del	NP_542158.1:p.Leu175_Ala177del
XM_005252105.2:c.449_457del	XP_005252162.1:p.Leu150_Ala152del
XM_011518875.1:c.449_457del	XP_011517177.1:p.Leu150_Ala152del
XM_011518876.1:c.197_205del	XP_011517178.1:p.Leu66_Ala68del
XM_005252105.3:c.449_457del	XP_005252162.1:p.Leu150_Ala152del
XM_011518875.2:c.449_457del	XP_011517177.1:p.Leu150_Ala152del
XM_011518876.2:c.197_205del	XP_011517178.1:p.Leu66_Ala68del
XM_024447614.1:c.197_205del	XP_024303382.1:p.Leu66_Ala68del
XM_024447615.1:c.197_205del	XP_024303383.1:p.Leu66_Ala68del
NM_000962.4:c.524_532del MANE Select	NP_000953.2:p.Leu175_Ala177del
NM_001271164.2:c.380_388del	NP_001258093.1:p.Leu127_Ala129del
NM_001271165.2:c.197_205del	NP_001258094.1:p.Leu66_Ala68del
NM_001271166.2:c.197_205del	NP_001258095.1:p.Leu66_Ala68del
NM_001271367.2:c.197_205del	NP_001258296.1:p.Leu66_Ala68del
NM_001271368.2:c.449_457del	NP_001258297.1:p.Leu150_Ala152del
NM_080591.3:c.524_532del	NP_542158.1:p.Leu175_Ala177del