Canonical Allele Identifier: CA260917282

Gene: PTGER2

Linked Data

• dbSNP Id: rs1056511040
• MyVariant Identifiers: chr14:g.52788881_52788886del (hg19) ; chr14:g.52322163_52322168del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52322172_52322177del , CM000676.2:g.52322172_52322177del	GRCh38
NC_000014.8:g.52788890_52788895del , CM000676.1:g.52788890_52788895del	GRCh37
NC_000014.7:g.51858640_51858645del	NCBI36
NG_013082.1:g.12875_12880del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-5049_844-5044del MANE Select	ENSP00000245457.5:n.844-5049_844-5044del
ENST00000245457.5:c.844-5049_844-5044del	ENSP00000245457.5:n.844-5049_844-5044del
ENST00000557436.1:c.79-5049_79-5044del	ENSP00000450933.1:n.79-5049_79-5044del
NM_000956.3:c.844-5049_844-5044del	NP_000947.2:n.844-5049_844-5044del
NM_000956.4:c.844-5049_844-5044del MANE Select	NP_000947.2:n.844-5049_844-5044del