Canonical Allele Identifier: CA24772134
Gene: PTGER3 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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