Canonical Allele Identifier: CA2137042300
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322443_52322444delinsCA , CM000676.2:g.52322443_52322444delinsCA GRCh38
NC_000014.8:g.52789161_52789162delinsCA , CM000676.1:g.52789161_52789162delinsCA GRCh37
NC_000014.7:g.51858911_51858912delinsCA NCBI36
NG_013082.1:g.13146_13147delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4778_844-4777delinsCA MANE Select ENSP00000245457.5:n.844-4778_844-4777delinsCA
ENST00000245457.5:c.844-4778_844-4777delinsCA ENSP00000245457.5:n.844-4778_844-4777delinsCA
ENST00000557436.1:c.79-4778_79-4777delinsCA ENSP00000450933.1:n.79-4778_79-4777delinsCA
NM_000956.3:c.844-4778_844-4777delinsCA NP_000947.2:n.844-4778_844-4777delinsCA
NM_000956.4:c.844-4778_844-4777delinsCA MANE Select NP_000947.2:n.844-4778_844-4777delinsCA