Canonical Allele Identifier: CA2137042269
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322422_52322424delinsCAA , CM000676.2:g.52322422_52322424delinsCAA GRCh38
NC_000014.8:g.52789140_52789142delinsCAA , CM000676.1:g.52789140_52789142delinsCAA GRCh37
NC_000014.7:g.51858890_51858892delinsCAA NCBI36
NG_013082.1:g.13125_13127delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4799_844-4797delinsCAA MANE Select ENSP00000245457.5:n.844-4799_844-4797delinsCAA
ENST00000245457.5:c.844-4799_844-4797delinsCAA ENSP00000245457.5:n.844-4799_844-4797delinsCAA
ENST00000557436.1:c.79-4799_79-4797delinsCAA ENSP00000450933.1:n.79-4799_79-4797delinsCAA
NM_000956.3:c.844-4799_844-4797delinsCAA NP_000947.2:n.844-4799_844-4797delinsCAA
NM_000956.4:c.844-4799_844-4797delinsCAA MANE Select NP_000947.2:n.844-4799_844-4797delinsCAA