Canonical Allele Identifier: CA1157335439
Gene: PLA2G2A HGNC NCBI

Linked Data

dbSNP Id: rs2046273591

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19979555G>A , CM000663.2:g.19979555G>A GRCh38
NC_000001.10:g.20306048G>A , CM000663.1:g.20306048G>A GRCh37
NC_000001.9:g.20178635G>A NCBI36
NG_012928.1:g.5885C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.-107+25C>T MANE Select ENSP00000504762.1:n.-107+25C>T
ENST00000400520.8:c.-139+25C>T ENSP00000383364.3:n.-139+25C>T
ENST00000482011.2:c.-107+25C>T ENSP00000504762.1:n.-107+25C>T
ENST00000649436.1:c.-148+25C>T ENSP00000496912.1:n.-148+25C>T
ENST00000375111.7:c.-107+25C>T ENSP00000364252.3:n.-107+25C>T
ENST00000400520.7:c.-107+25C>T ENSP00000383364.3:n.-107+25C>T
ENST00000469162.5:n.28+25C>T
ENST00000482011.1:n.166+25C>T
ENST00000491964.5:n.126+25C>T
ENST00000496748.1:n.35+25C>T
NM_000300.3:c.-107+25C>T NP_000291.1:n.-107+25C>T
NM_001161727.1:c.-107+25C>T NP_001155199.1:n.-107+25C>T
NM_001161728.1:c.-106-676C>T NP_001155200.1:n.-106-676C>T
NM_001161729.1:c.-139+25C>T NP_001155201.1:n.-139+25C>T
NM_000300.4:c.-107+25C>T NP_000291.1:n.-107+25C>T
NM_001161727.2:c.-107+25C>T NP_001155199.1:n.-107+25C>T
NM_001161728.2:c.-106-676C>T NP_001155200.1:n.-106-676C>T
NM_001395463.1:c.-107+25C>T MANE Select NP_001382392.1:n.-107+25C>T