Canonical Allele Identifier: CA339253854
Gene: PLA2G2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978464C>G , CM000663.2:g.19978464C>G GRCh38
NC_000001.10:g.20304957C>G , CM000663.1:g.20304957C>G GRCh37
NC_000001.9:g.20177544C>G NCBI36
NG_012928.1:g.6976G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.101G>C MANE Select ENSP00000504762.1:p.Gly34Ala
ENST00000400520.8:c.101G>C ENSP00000383364.3:p.Gly34Ala
ENST00000482011.2:c.101G>C ENSP00000504762.1:p.Gly34Ala
ENST00000649436.1:c.20G>C ENSP00000496912.1:p.Gly7Ala
ENST00000375111.7:c.101G>C ENSP00000364252.3:p.Gly34Ala
ENST00000400520.7:c.101G>C ENSP00000383364.3:p.Gly34Ala
ENST00000461140.1:n.355G>C
ENST00000469162.5:n.267G>C
ENST00000482011.1:n.373G>C
ENST00000491964.5:n.333G>C
ENST00000496748.1:n.451G>C
NM_000300.3:c.101G>C NP_000291.1:p.Gly34Ala
NM_001161727.1:c.101G>C NP_001155199.1:p.Gly34Ala
NM_001161728.1:c.101G>C NP_001155200.1:p.Gly34Ala
NM_001161729.1:c.101G>C NP_001155201.1:p.Gly34Ala
NM_000300.4:c.101G>C NP_000291.1:p.Gly34Ala
NM_001161727.2:c.101G>C NP_001155199.1:p.Gly34Ala
NM_001161728.2:c.101G>C NP_001155200.1:p.Gly34Ala
NM_001395463.1:c.101G>C MANE Select NP_001382392.1:p.Gly34Ala