Canonical Allele Identifier: CA1157333355
Gene: PLA2G2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978151G= , CM000663.2:g.19978151G= GRCh38
NC_000001.10:g.20304644G= , CM000663.1:g.20304644G= GRCh37
NC_000001.9:g.20177231G= NCBI36
NG_012928.1:g.7289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.186-30C= MANE Select ENSP00000504762.1:n.186-30C=
ENST00000400520.8:c.186-30C= ENSP00000383364.3:n.186-30C=
ENST00000482011.2:c.186-30C= ENSP00000504762.1:n.186-30C=
ENST00000649436.1:c.105-30C= ENSP00000496912.1:n.105-30C=
ENST00000375111.7:c.186-30C= ENSP00000364252.3:n.186-30C=
ENST00000400520.7:c.186-30C= ENSP00000383364.3:n.186-30C=
ENST00000469162.5:n.352-30C=
ENST00000482011.1:n.458-30C=
ENST00000491964.5:n.418-30C=
ENST00000496748.1:n.764C=
NM_000300.3:c.186-30C= NP_000291.1:n.186-30C=
NM_001161727.1:c.186-30C= NP_001155199.1:n.186-30C=
NM_001161728.1:c.186-30C= NP_001155200.1:n.186-30C=
NM_001161729.1:c.186-30C= NP_001155201.1:n.186-30C=
NM_000300.4:c.186-30C= NP_000291.1:n.186-30C=
NM_001161727.2:c.186-30C= NP_001155199.1:n.186-30C=
NM_001161728.2:c.186-30C= NP_001155200.1:n.186-30C=
NM_001395463.1:c.186-30C= MANE Select NP_001382392.1:n.186-30C=