Canonical Allele Identifier: CA10773444
Gene: PTGER3 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.70964785G>T , CM000663.2:g.70964785G>T GRCh38
NC_000001.10:g.71430468G>T , CM000663.1:g.71430468G>T GRCh37
NC_000001.9:g.71203056G>T NCBI36
NG_029509.1:g.88024C>A
NG_029509.2:g.88024C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356595.8:c.1078-10996C>A ENSP00000349003.4:n.1078-10996C>A
ENST00000361210.6:c.1078-10996C>A ENSP00000424340.1:n.1078-10996C>A
ENST00000370931.7:c.1169+9512C>A ENSP00000359969.3:n.1169+9512C>A
ENST00000370932.6:c.1094+47503C>A ENSP00000359970.3:n.1094+47503C>A
ENST00000460330.5:c.1078-10996C>A ENSP00000418073.1:n.1078-10996C>A
ENST00000479353.5:c.1077+47520C>A ENSP00000421583.1:n.1077+47520C>A
ENST00000497146.5:c.1078-10996C>A ENSP00000423561.1:n.1078-10996C>A
ENST00000628037.2:c.1077+47520C>A ENSP00000486617.1:n.1077+47520C>A
NM_001126044.1:c.1169+9512C>A NP_001119516.1:n.1169+9512C>A
NM_198714.1:c.1169+9512C>A NP_942007.1:n.1169+9512C>A
NM_198716.1:c.1078-10996C>A NP_942009.1:n.1078-10996C>A
NM_198717.1:c.1077+47520C>A NP_942010.1:n.1077+47520C>A
NM_198718.1:c.1078-10996C>A NP_942011.1:n.1078-10996C>A
NR_028292.1:n.1309-10996C>A
NR_028293.1:n.1308+47520C>A
NR_028294.1:n.1309-10996C>A
XM_011541809.1:c.1078-10996C>A XP_011540111.1:n.1078-10996C>A
XM_011541810.1:c.1169+9512C>A XP_011540112.1:n.1169+9512C>A
XM_011541811.1:c.1078-10996C>A XP_011540113.1:n.1078-10996C>A
XR_946714.1:n.1315-10996C>A
XM_011541810.3:c.1169+9512C>A XP_011540112.1:n.1169+9512C>A
XR_001737666.1:n.1939-61G>T
XR_001737667.1:n.1635-61G>T
XR_946714.2:n.1309-10996C>A
NM_001126044.2:c.1169+9512C>A NP_001119516.1:n.1169+9512C>A
NM_198714.2:c.1169+9512C>A NP_942007.1:n.1169+9512C>A
NM_198716.2:c.1078-10996C>A NP_942009.1:n.1078-10996C>A
NM_198717.2:c.1077+47520C>A NP_942010.1:n.1077+47520C>A
NM_198718.2:c.1078-10996C>A NP_942011.1:n.1078-10996C>A
NR_028292.2:n.1317-10996C>A
NR_028293.2:n.1316+47520C>A
NR_028294.2:n.1317-10996C>A