Canonical Allele Identifier: CA2509750844
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322145_52322146insCTTGAA , CM000676.2:g.52322145_52322146insCTTGAA GRCh38
NC_000014.8:g.52788863_52788864insCTTGAA , CM000676.1:g.52788863_52788864insCTTGAA GRCh37
NC_000014.7:g.51858613_51858614insCTTGAA NCBI36
NG_013082.1:g.12848_12849insCTTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5076_844-5075insCTTGAA MANE Select ENSP00000245457.5:n.844-5076_844-5075insCTTGAA
ENST00000245457.5:c.844-5076_844-5075insCTTGAA ENSP00000245457.5:n.844-5076_844-5075insCTTGAA
ENST00000557436.1:c.79-5076_79-5075insCTTGAA ENSP00000450933.1:n.79-5076_79-5075insCTTGAA
NM_000956.3:c.844-5076_844-5075insCTTGAA NP_000947.2:n.844-5076_844-5075insCTTGAA
NM_000956.4:c.844-5076_844-5075insCTTGAA MANE Select NP_000947.2:n.844-5076_844-5075insCTTGAA