Canonical Allele Identifier: CA1877496539

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381373_122381379delinsAAGAAGC , CM000671.2:g.122381373_122381379delinsAAGAAGC	GRCh38
NC_000009.11:g.125143652_125143658delinsAAGAAGC , CM000671.1:g.125143652_125143658delinsAAGAAGC	GRCh37
NC_000009.10:g.124183473_124183479delinsAAGAAGC	NCBI36
NG_032900.1:g.15424_15430delinsAAGAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.499_505delinsAAGAAGC MANE Select	ENSP00000354612.2:p.Lys167=
ENST00000373698.7:c.172_178delinsAAGAAGC	ENSP00000362802.5:p.Lys58=
ENST00000426608.6:c.313-123_313-117delinsAAGAAGC	ENSP00000411606.2:n.313-123_313-117delinsAAGAAGC
ENST00000540753.6:c.424_430delinsAAGAAGC	ENSP00000437709.1:p.Lys142=
ENST00000619306.5:c.355_361delinsAAGAAGC	ENSP00000483540.2:p.Lys119=
ENST00000643576.1:n.593_599delinsAAGAAGC
ENST00000643810.1:c.172_178delinsAAGAAGC	ENSP00000494717.1:p.Lys58=
ENST00000645132.1:n.519+2800_519+2806delinsAAGAAGC
ENST00000647067.1:c.*344_*350delinsAAGAAGC	ENSP00000495728.1:n.*344_*350delinsAAGAAGC
ENST00000223423.8:c.499_505delinsAAGAAGC	ENSP00000223423.4:p.Lys167=
ENST00000362012.6:c.499_505delinsAAGAAGC	ENSP00000354612.2:p.Lys167=
ENST00000373698.6:c.172_178delinsAAGAAGC	ENSP00000362802.5:p.Lys58=
ENST00000426608.5:c.304-123_304-117delinsAAGAAGC	ENSP00000411606.1:n.304-123_304-117delinsAAGAAGC
ENST00000540753.5:c.424_430delinsAAGAAGC	ENSP00000437709.1:p.Lys142=
ENST00000614910.4:c.355_361delinsAAGAAGC	ENSP00000484800.1:p.Lys119=
ENST00000619306.4:c.592_598delinsAAGAAGC	ENSP00000483540.1:p.Lys198=
NM_000962.3:c.499_505delinsAAGAAGC	NP_000953.2:p.Lys167=
NM_001271164.1:c.355_361delinsAAGAAGC	NP_001258093.1:p.Lys119=
NM_001271165.1:c.172_178delinsAAGAAGC	NP_001258094.1:p.Lys58=
NM_001271166.1:c.172_178delinsAAGAAGC	NP_001258095.1:p.Lys58=
NM_001271367.1:c.172_178delinsAAGAAGC	NP_001258296.1:p.Lys58=
NM_001271368.1:c.424_430delinsAAGAAGC	NP_001258297.1:p.Lys142=
NM_080591.2:c.499_505delinsAAGAAGC	NP_542158.1:p.Lys167=
XM_005252105.2:c.424_430delinsAAGAAGC	XP_005252162.1:p.Lys142=
XM_011518875.1:c.424_430delinsAAGAAGC	XP_011517177.1:p.Lys142=
XM_011518876.1:c.172_178delinsAAGAAGC	XP_011517178.1:p.Lys58=
XM_005252105.3:c.424_430delinsAAGAAGC	XP_005252162.1:p.Lys142=
XM_011518875.2:c.424_430delinsAAGAAGC	XP_011517177.1:p.Lys142=
XM_011518876.2:c.172_178delinsAAGAAGC	XP_011517178.1:p.Lys58=
XM_024447614.1:c.172_178delinsAAGAAGC	XP_024303382.1:p.Lys58=
XM_024447615.1:c.172_178delinsAAGAAGC	XP_024303383.1:p.Lys58=
NM_000962.4:c.499_505delinsAAGAAGC MANE Select	NP_000953.2:p.Lys167=
NM_001271164.2:c.355_361delinsAAGAAGC	NP_001258093.1:p.Lys119=
NM_001271165.2:c.172_178delinsAAGAAGC	NP_001258094.1:p.Lys58=
NM_001271166.2:c.172_178delinsAAGAAGC	NP_001258095.1:p.Lys58=
NM_001271367.2:c.172_178delinsAAGAAGC	NP_001258296.1:p.Lys58=
NM_001271368.2:c.424_430delinsAAGAAGC	NP_001258297.1:p.Lys142=
NM_080591.3:c.499_505delinsAAGAAGC	NP_542158.1:p.Lys167=