Canonical Allele Identifier: CA1139844870

Gene: PTGER3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70960577A= , CM000663.2:g.70960577A=	GRCh38
NC_000001.10:g.71426260A= , CM000663.1:g.71426260A=	GRCh37
NC_000001.9:g.71198848A=	NCBI36
NG_029509.1:g.92232T=
NG_029509.2:g.92232T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356595.8:c.1078-6788T=	ENSP00000349003.4:n.1078-6788T=
ENST00000361210.6:c.1078-6788T=	ENSP00000424340.1:n.1078-6788T=
ENST00000370931.7:c.1170-6788T=	ENSP00000359969.3:n.1170-6788T=
ENST00000370932.6:c.1094+51711T=	ENSP00000359970.3:n.1094+51711T=
ENST00000460330.5:c.1078-6788T=	ENSP00000418073.1:n.1078-6788T=
ENST00000479353.5:c.1077+51728T=	ENSP00000421583.1:n.1077+51728T=
ENST00000497146.5:c.1078-6788T=	ENSP00000423561.1:n.1078-6788T=
ENST00000628037.2:c.1077+51728T=	ENSP00000486617.1:n.1077+51728T=
NM_001126044.1:c.1170-6788T=	NP_001119516.1:n.1170-6788T=
NM_198714.1:c.1170-6788T=	NP_942007.1:n.1170-6788T=
NM_198716.1:c.1078-6788T=	NP_942009.1:n.1078-6788T=
NM_198717.1:c.1077+51728T=	NP_942010.1:n.1077+51728T=
NM_198718.1:c.1078-6788T=	NP_942011.1:n.1078-6788T=
NR_028292.1:n.1309-6788T=
NR_028293.1:n.1308+51728T=
NR_028294.1:n.1309-6788T=
XM_011541809.1:c.1078-6788T=	XP_011540111.1:n.1078-6788T=
XM_011541810.1:c.1169+13720T=	XP_011540112.1:n.1169+13720T=
XM_011541811.1:c.1078-6788T=	XP_011540113.1:n.1078-6788T=
XR_946714.1:n.1315-6788T=
XM_011541810.3:c.1169+13720T=	XP_011540112.1:n.1169+13720T=
XR_001737666.1:n.953A=
XR_001737667.1:n.953A=
XR_946714.2:n.1309-6788T=
NM_001126044.2:c.1170-6788T=	NP_001119516.1:n.1170-6788T=
NM_198714.2:c.1170-6788T=	NP_942007.1:n.1170-6788T=
NM_198716.2:c.1078-6788T=	NP_942009.1:n.1078-6788T=
NM_198717.2:c.1077+51728T=	NP_942010.1:n.1077+51728T=
NM_198718.2:c.1078-6788T=	NP_942011.1:n.1078-6788T=
NR_028292.2:n.1317-6788T=
NR_028293.2:n.1316+51728T=
NR_028294.2:n.1317-6788T=