Canonical Allele Identifier: CA2339003878

Gene: PTGIR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46623592G= , CM000681.2:g.46623592G=	GRCh38
NC_000019.9:g.47126849G= , CM000681.1:g.47126849G=	GRCh37
NC_000019.8:g.51818689G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000960.4:c.634C= MANE Select	NP_000951.1:p.Arg212=
ENST00000291294.7:c.634C= MANE Select	ENSP00000291294.1:p.Arg212=
NM_000960.3:c.634C=	NP_000951.1:p.Arg212=
ENST00000291294.6:c.634C=	ENSP00000291294.1:p.Arg212=
ENST00000594275.1:c.-78-18C=	ENSP00000469408.1:n.-78-18C=
ENST00000595460.1:n.1156C=
ENST00000596260.1:c.634C=	ENSP00000468970.1:p.Arg212=
ENST00000597185.1:c.-195+1361C=	ENSP00000470566.1:n.-195+1361C=
ENST00000598865.5:c.-3C=	ENSP00000470799.1:n.-3C=
XM_005259093.2:c.634C=	XP_005259150.1:p.Arg212=
XM_005259093.3:c.634C=	XP_005259150.1:p.Arg212=
XM_005259095.2:c.634C=	XP_005259152.1:p.Arg212=
XM_005259095.4:c.634C=	XP_005259152.1:p.Arg212=
XR_243945.2:n.768C=
XR_243945.3:n.742C=
XR_430206.2:n.768C=
XR_430206.3:n.742C=
XR_935844.1:n.768C=
XR_935844.2:n.742C=