Canonical Allele Identifier: CA2561169058
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322098_52322099insAAGGTTTGTAAA , CM000676.2:g.52322098_52322099insAAGGTTTGTAAA GRCh38
NC_000014.8:g.52788816_52788817insAAGGTTTGTAAA , CM000676.1:g.52788816_52788817insAAGGTTTGTAAA GRCh37
NC_000014.7:g.51858566_51858567insAAGGTTTGTAAA NCBI36
NG_013082.1:g.12801_12802insAAGGTTTGTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5123_844-5122insAAGGTTTGTAAA MANE Select ENSP00000245457.5:n.844-5123_844-5122insAAGGTTTGTAAA
ENST00000245457.5:c.844-5123_844-5122insAAGGTTTGTAAA ENSP00000245457.5:n.844-5123_844-5122insAAGGTTTGTAAA
ENST00000557436.1:c.79-5123_79-5122insAAGGTTTGTAAA ENSP00000450933.1:n.79-5123_79-5122insAAGGTTTGTAAA
NM_000956.3:c.844-5123_844-5122insAAGGTTTGTAAA NP_000947.2:n.844-5123_844-5122insAAGGTTTGTAAA
NM_000956.4:c.844-5123_844-5122insAAGGTTTGTAAA MANE Select NP_000947.2:n.844-5123_844-5122insAAGGTTTGTAAA