Canonical Allele Identifier: CA1872568534

Gene: PTGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.111586337C= , CM000671.2:g.111586337C=	GRCh38
NC_000009.11:g.114348617C= , CM000671.1:g.114348617C=	GRCh37
NC_000009.10:g.113388438C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407693.7:c.210-172G= MANE Select	ENSP00000385763.2:n.210-172G=
ENST00000466771.6:c.210-172G=	ENSP00000435665.2:n.210-172G=
ENST00000538962.7:c.210-172G=	ENSP00000440281.1:n.210-172G=
ENST00000309195.9:c.210-172G=	ENSP00000311572.5:n.210-172G=
ENST00000374324.5:c.*107-172G=	ENSP00000363444.1:n.*107-172G=
ENST00000407693.6:c.210-172G=	ENSP00000385763.2:n.210-172G=
ENST00000422125.1:c.153-172G=	ENSP00000395965.1:n.153-172G=
ENST00000538962.5:c.210-172G=	ENSP00000440281.1:n.210-172G=
NM_001146108.1:c.210-172G=	NP_001139580.1:n.210-172G=
NM_001146109.1:c.210-172G=	NP_001139581.1:n.210-172G=
NM_012212.3:c.210-172G=	NP_036344.2:n.210-172G=
XM_011518394.1:c.210-172G=	XP_011516696.1:n.210-172G=
XM_011518395.1:c.-160-172G=	XP_011516697.1:n.-160-172G=
XR_929738.1:n.473-172G=
XM_011518394.2:c.210-172G=	XP_011516696.1:n.210-172G=
XM_011518395.3:c.-160-172G=	XP_011516697.1:n.-160-172G=
XM_017014485.2:c.210-172G=	XP_016869974.1:n.210-172G=
XR_001746250.2:n.311-172G=
XR_929738.2:n.473-172G=
NM_001146108.2:c.210-172G= MANE Select	NP_001139580.1:n.210-172G=
NM_001146109.2:c.210-172G=	NP_001139581.1:n.210-172G=