Canonical Allele Identifier: CA2581388051

Gene: PTGIR

Genomic Alleles

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

Transcript Alleles

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