Canonical Allele Identifier: CA1174647400

Gene: PTGER3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70989465C= , CM000663.2:g.70989465C=	GRCh38
NC_000001.10:g.71455148C= , CM000663.1:g.71455148C=	GRCh37
NC_000001.9:g.71227736C=	NCBI36
NG_029509.1:g.63344G=
NG_029509.2:g.63344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306666.10:c.1078-15077G= MANE Select	ENSP00000302313.5:n.1078-15077G=
ENST00000306666.9:c.1078-15077G=	ENSP00000302313.5:n.1078-15077G=
ENST00000351052.9:c.1078-15077G=	ENSP00000280208.8:n.1078-15077G=
ENST00000356595.8:c.1077+22840G=	ENSP00000349003.4:n.1077+22840G=
ENST00000361210.6:c.1077+22840G=	ENSP00000424340.1:n.1077+22840G=
ENST00000370931.7:c.1078-15077G=	ENSP00000359969.3:n.1078-15077G=
ENST00000370932.6:c.1094+22823G=	ENSP00000359970.3:n.1094+22823G=
ENST00000460330.5:c.1077+22840G=	ENSP00000418073.1:n.1077+22840G=
ENST00000479353.5:c.1077+22840G=	ENSP00000421583.1:n.1077+22840G=
ENST00000497146.5:c.1077+22840G=	ENSP00000423561.1:n.1077+22840G=
ENST00000628037.2:c.1077+22840G=	ENSP00000486617.1:n.1077+22840G=
NM_001126044.1:c.1078-15077G=	NP_001119516.1:n.1078-15077G=
NM_198714.1:c.1078-15077G=	NP_942007.1:n.1078-15077G=
NM_198716.1:c.1077+22840G=	NP_942009.1:n.1077+22840G=
NM_198717.1:c.1077+22840G=	NP_942010.1:n.1077+22840G=
NM_198718.1:c.1077+22840G=	NP_942011.1:n.1077+22840G=
NM_198719.1:c.1078-15077G=	NP_942012.1:n.1078-15077G=
NR_028292.1:n.1308+22840G=
NR_028293.1:n.1308+22840G=
NR_028294.1:n.1308+22840G=
XM_011541809.1:c.1077+22840G=	XP_011540111.1:n.1077+22840G=
XM_011541810.1:c.1078-15077G=	XP_011540112.1:n.1078-15077G=
XM_011541811.1:c.1077+22840G=	XP_011540113.1:n.1077+22840G=
XR_946714.1:n.1314+22840G=
XM_011541810.3:c.1078-15077G=	XP_011540112.1:n.1078-15077G=
XR_946714.2:n.1308+22840G=
NM_001126044.2:c.1078-15077G=	NP_001119516.1:n.1078-15077G=
NM_198714.2:c.1078-15077G=	NP_942007.1:n.1078-15077G=
NM_198716.2:c.1077+22840G=	NP_942009.1:n.1077+22840G=
NM_198717.2:c.1077+22840G=	NP_942010.1:n.1077+22840G=
NM_198718.2:c.1077+22840G=	NP_942011.1:n.1077+22840G=
NM_198719.2:c.1078-15077G= MANE Select	NP_942012.1:n.1078-15077G=
NR_028292.2:n.1316+22840G=
NR_028293.2:n.1316+22840G=
NR_028294.2:n.1316+22840G=