Canonical Allele Identifier: CA1157333836
Gene: PLA2G2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978423_19978432delinsAGTGGCAGCC , CM000663.2:g.19978423_19978432delinsAGTGGCAGCC GRCh38
NC_000001.10:g.20304916_20304925delinsAGTGGCAGCC , CM000663.1:g.20304916_20304925delinsAGTGGCAGCC GRCh37
NC_000001.9:g.20177503_20177512delinsAGTGGCAGCC NCBI36
NG_012928.1:g.7008_7017delinsGGCTGCCACT

Transcript Alleles

HGVS Amino-acid change
ENST00000482011.3:c.133_142delinsGGCTGCCACT MANE Select ENSP00000504762.1:p.Gly45=
ENST00000400520.8:c.133_142delinsGGCTGCCACT ENSP00000383364.3:p.Gly45=
ENST00000482011.2:c.133_142delinsGGCTGCCACT ENSP00000504762.1:p.Gly45=
ENST00000649436.1:c.52_61delinsGGCTGCCACT ENSP00000496912.1:p.Gly18=
ENST00000375111.7:c.133_142delinsGGCTGCCACT ENSP00000364252.3:p.Gly45=
ENST00000400520.7:c.133_142delinsGGCTGCCACT ENSP00000383364.3:p.Gly45=
ENST00000461140.1:n.387_396delinsGGCTGCCACT
ENST00000469162.5:n.299_308delinsGGCTGCCACT
ENST00000482011.1:n.405_414delinsGGCTGCCACT
ENST00000491964.5:n.365_374delinsGGCTGCCACT
ENST00000496748.1:n.483_492delinsGGCTGCCACT
NM_000300.3:c.133_142delinsGGCTGCCACT NP_000291.1:p.Gly45=
NM_001161727.1:c.133_142delinsGGCTGCCACT NP_001155199.1:p.Gly45=
NM_001161728.1:c.133_142delinsGGCTGCCACT NP_001155200.1:p.Gly45=
NM_001161729.1:c.133_142delinsGGCTGCCACT NP_001155201.1:p.Gly45=
NM_000300.4:c.133_142delinsGGCTGCCACT NP_000291.1:p.Gly45=
NM_001161727.2:c.133_142delinsGGCTGCCACT NP_001155199.1:p.Gly45=
NM_001161728.2:c.133_142delinsGGCTGCCACT NP_001155200.1:p.Gly45=
NM_001395463.1:c.133_142delinsGGCTGCCACT MANE Select NP_001382392.1:p.Gly45=