Canonical Allele Identifier: CA2137042263

Gene: PTGER2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52322421_52322448delinsACAAAGATCACAAGGCAAAGGGCAAAAG , CM000676.2:g.52322421_52322448delinsACAAAGATCACAAGGCAAAGGGCAAAAG	GRCh38
NC_000014.8:g.52789139_52789166delinsACAAAGATCACAAGGCAAAGGGCAAAAG , CM000676.1:g.52789139_52789166delinsACAAAGATCACAAGGCAAAGGGCAAAAG	GRCh37
NC_000014.7:g.51858889_51858916delinsACAAAGATCACAAGGCAAAGGGCAAAAG	NCBI36
NG_013082.1:g.13124_13151delinsACAAAGATCACAAGGCAAAGGGCAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG MANE Select	ENSP00000245457.5:n.844-4800_844-4773delinsACAAAGATCACAAGGCAA...
ENST00000245457.5:c.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG	ENSP00000245457.5:n.844-4800_844-4773delinsACAAAGATCACAAGGCAA...
ENST00000557436.1:c.79-4800_79-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG	ENSP00000450933.1:n.79-4800_79-4773delinsACAAAGATCACAAGGCAAAG...
NM_000956.3:c.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG	NP_000947.2:n.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCA...
NM_000956.4:c.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG MANE Select	NP_000947.2:n.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCA...