Canonical Allele Identifier: CA339253839
Gene: PLA2G2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978458T>G , CM000663.2:g.19978458T>G GRCh38
NC_000001.10:g.20304951T>G , CM000663.1:g.20304951T>G GRCh37
NC_000001.9:g.20177538T>G NCBI36
NG_012928.1:g.6982A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.107A>C MANE Select ENSP00000504762.1:p.Glu36Ala
ENST00000400520.8:c.107A>C ENSP00000383364.3:p.Glu36Ala
ENST00000482011.2:c.107A>C ENSP00000504762.1:p.Glu36Ala
ENST00000649436.1:c.26A>C ENSP00000496912.1:p.Glu9Ala
ENST00000375111.7:c.107A>C ENSP00000364252.3:p.Glu36Ala
ENST00000400520.7:c.107A>C ENSP00000383364.3:p.Glu36Ala
ENST00000461140.1:n.361A>C
ENST00000469162.5:n.273A>C
ENST00000482011.1:n.379A>C
ENST00000491964.5:n.339A>C
ENST00000496748.1:n.457A>C
NM_000300.3:c.107A>C NP_000291.1:p.Glu36Ala
NM_001161727.1:c.107A>C NP_001155199.1:p.Glu36Ala
NM_001161728.1:c.107A>C NP_001155200.1:p.Glu36Ala
NM_001161729.1:c.107A>C NP_001155201.1:p.Glu36Ala
NM_000300.4:c.107A>C NP_000291.1:p.Glu36Ala
NM_001161727.2:c.107A>C NP_001155199.1:p.Glu36Ala
NM_001161728.2:c.107A>C NP_001155200.1:p.Glu36Ala
NM_001395463.1:c.107A>C MANE Select NP_001382392.1:p.Glu36Ala