Canonical Allele Identifier: CA2339002414

Gene: PTGIR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46620526A= , CM000681.2:g.46620526A=	GRCh38
NC_000019.9:g.47123783A= , CM000681.1:g.47123783A=	GRCh37
NC_000019.8:g.51815623A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000960.4:c.*754T= MANE Select	NP_000951.1:n.*754T=
ENST00000291294.7:c.*754T= MANE Select	ENSP00000291294.1:n.*754T=
NM_000960.3:c.*754T=	NP_000951.1:n.*754T=
ENST00000291294.6:c.*754T=	ENSP00000291294.1:n.*754T=
XM_005259093.2:c.*1595T=	XP_005259150.1:n.*1595T=
XM_005259093.3:c.*1595T=	XP_005259150.1:n.*1595T=
XM_005259095.4:c.*1103T=	XP_005259152.1:n.*1103T=
XR_243945.2:n.902+2932T=
XR_243945.3:n.876+2932T=
XR_430206.2:n.902+2932T=
XR_430206.3:n.876+2932T=
XR_935844.1:n.902+2932T=
XR_935844.2:n.876+2932T=