Canonical Allele Identifier: CA2137041948
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322182_52322184delinsAAG , CM000676.2:g.52322182_52322184delinsAAG GRCh38
NC_000014.8:g.52788900_52788902delinsAAG , CM000676.1:g.52788900_52788902delinsAAG GRCh37
NC_000014.7:g.51858650_51858652delinsAAG NCBI36
NG_013082.1:g.12885_12887delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5039_844-5037delinsAAG MANE Select ENSP00000245457.5:n.844-5039_844-5037delinsAAG
ENST00000245457.5:c.844-5039_844-5037delinsAAG ENSP00000245457.5:n.844-5039_844-5037delinsAAG
ENST00000557436.1:c.79-5039_79-5037delinsAAG ENSP00000450933.1:n.79-5039_79-5037delinsAAG
NM_000956.3:c.844-5039_844-5037delinsAAG NP_000947.2:n.844-5039_844-5037delinsAAG
NM_000956.4:c.844-5039_844-5037delinsAAG MANE Select NP_000947.2:n.844-5039_844-5037delinsAAG