Canonical Allele Identifier: CA339253868
Gene: PLA2G2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978471T>G , CM000663.2:g.19978471T>G GRCh38
NC_000001.10:g.20304964T>G , CM000663.1:g.20304964T>G GRCh37
NC_000001.9:g.20177551T>G NCBI36
NG_012928.1:g.6969A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.94A>C MANE Select ENSP00000504762.1:p.Thr32Pro
ENST00000400520.8:c.94A>C ENSP00000383364.3:p.Thr32Pro
ENST00000482011.2:c.94A>C ENSP00000504762.1:p.Thr32Pro
ENST00000649436.1:c.13A>C ENSP00000496912.1:p.Thr5Pro
ENST00000375111.7:c.94A>C ENSP00000364252.3:p.Thr32Pro
ENST00000400520.7:c.94A>C ENSP00000383364.3:p.Thr32Pro
ENST00000461140.1:n.348A>C
ENST00000469162.5:n.260A>C
ENST00000482011.1:n.366A>C
ENST00000491964.5:n.326A>C
ENST00000496748.1:n.444A>C
NM_000300.3:c.94A>C NP_000291.1:p.Thr32Pro
NM_001161727.1:c.94A>C NP_001155199.1:p.Thr32Pro
NM_001161728.1:c.94A>C NP_001155200.1:p.Thr32Pro
NM_001161729.1:c.94A>C NP_001155201.1:p.Thr32Pro
NM_000300.4:c.94A>C NP_000291.1:p.Thr32Pro
NM_001161727.2:c.94A>C NP_001155199.1:p.Thr32Pro
NM_001161728.2:c.94A>C NP_001155200.1:p.Thr32Pro
NM_001395463.1:c.94A>C MANE Select NP_001382392.1:p.Thr32Pro