Canonical Allele Identifier: CA1174647417

Gene: PTGER3

Linked Data

• dbSNP Id: rs1655234693

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.70989504_70989506del , CM000663.2:g.70989504_70989506del	GRCh38
NC_000001.10:g.71455187_71455189del , CM000663.1:g.71455187_71455189del	GRCh37
NC_000001.9:g.71227775_71227777del	NCBI36
NG_029509.1:g.63306_63308del
NG_029509.2:g.63306_63308del

Transcript Alleles

HGVS	Amino-acid change
ENST00000306666.10:c.1078-15115_1078-15113del MANE Select	ENSP00000302313.5:n.1078-15115_1078-15113del
ENST00000306666.9:c.1078-15115_1078-15113del	ENSP00000302313.5:n.1078-15115_1078-15113del
ENST00000351052.9:c.1078-15115_1078-15113del	ENSP00000280208.8:n.1078-15115_1078-15113del
ENST00000356595.8:c.1077+22802_1077+22804del	ENSP00000349003.4:n.1077+22802_1077+22804del
ENST00000361210.6:c.1077+22802_1077+22804del	ENSP00000424340.1:n.1077+22802_1077+22804del
ENST00000370931.7:c.1078-15115_1078-15113del	ENSP00000359969.3:n.1078-15115_1078-15113del
ENST00000370932.6:c.1094+22785_1094+22787del	ENSP00000359970.3:n.1094+22785_1094+22787del
ENST00000460330.5:c.1077+22802_1077+22804del	ENSP00000418073.1:n.1077+22802_1077+22804del
ENST00000479353.5:c.1077+22802_1077+22804del	ENSP00000421583.1:n.1077+22802_1077+22804del
ENST00000497146.5:c.1077+22802_1077+22804del	ENSP00000423561.1:n.1077+22802_1077+22804del
ENST00000628037.2:c.1077+22802_1077+22804del	ENSP00000486617.1:n.1077+22802_1077+22804del
NM_001126044.1:c.1078-15115_1078-15113del	NP_001119516.1:n.1078-15115_1078-15113del
NM_198714.1:c.1078-15115_1078-15113del	NP_942007.1:n.1078-15115_1078-15113del
NM_198716.1:c.1077+22802_1077+22804del	NP_942009.1:n.1077+22802_1077+22804del
NM_198717.1:c.1077+22802_1077+22804del	NP_942010.1:n.1077+22802_1077+22804del
NM_198718.1:c.1077+22802_1077+22804del	NP_942011.1:n.1077+22802_1077+22804del
NM_198719.1:c.1078-15115_1078-15113del	NP_942012.1:n.1078-15115_1078-15113del
NR_028292.1:n.1308+22802_1308+22804del
NR_028293.1:n.1308+22802_1308+22804del
NR_028294.1:n.1308+22802_1308+22804del
XM_011541809.1:c.1077+22802_1077+22804del	XP_011540111.1:n.1077+22802_1077+22804del
XM_011541810.1:c.1078-15115_1078-15113del	XP_011540112.1:n.1078-15115_1078-15113del
XM_011541811.1:c.1077+22802_1077+22804del	XP_011540113.1:n.1077+22802_1077+22804del
XR_946714.1:n.1314+22802_1314+22804del
XM_011541810.3:c.1078-15115_1078-15113del	XP_011540112.1:n.1078-15115_1078-15113del
XR_946714.2:n.1308+22802_1308+22804del
NM_001126044.2:c.1078-15115_1078-15113del	NP_001119516.1:n.1078-15115_1078-15113del
NM_198714.2:c.1078-15115_1078-15113del	NP_942007.1:n.1078-15115_1078-15113del
NM_198716.2:c.1077+22802_1077+22804del	NP_942009.1:n.1077+22802_1077+22804del
NM_198717.2:c.1077+22802_1077+22804del	NP_942010.1:n.1077+22802_1077+22804del
NM_198718.2:c.1077+22802_1077+22804del	NP_942011.1:n.1077+22802_1077+22804del
NM_198719.2:c.1078-15115_1078-15113del MANE Select	NP_942012.1:n.1078-15115_1078-15113del
NR_028292.2:n.1316+22802_1316+22804del
NR_028293.2:n.1316+22802_1316+22804del
NR_028294.2:n.1316+22802_1316+22804del