Canonical Allele Identifier: CA2643828345

Gene: PLA2G2A

Linked Data

• gnomAD v4: 1-19979561-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19979561A>G , CM000663.2:g.19979561A>G	GRCh38
NC_000001.10:g.20306054A>G , CM000663.1:g.20306054A>G	GRCh37
NC_000001.9:g.20178641A>G	NCBI36
NG_012928.1:g.5879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.-107+19T>C MANE Select	ENSP00000504762.1:n.-107+19T>C
ENST00000400520.8:c.-139+19T>C	ENSP00000383364.3:n.-139+19T>C
ENST00000482011.2:c.-107+19T>C	ENSP00000504762.1:n.-107+19T>C
ENST00000649436.1:c.-148+19T>C	ENSP00000496912.1:n.-148+19T>C
ENST00000375111.7:c.-107+19T>C	ENSP00000364252.3:n.-107+19T>C
ENST00000400520.7:c.-107+19T>C	ENSP00000383364.3:n.-107+19T>C
ENST00000469162.5:n.28+19T>C
ENST00000482011.1:n.166+19T>C
ENST00000491964.5:n.126+19T>C
ENST00000496748.1:n.35+19T>C
NM_000300.3:c.-107+19T>C	NP_000291.1:n.-107+19T>C
NM_001161727.1:c.-107+19T>C	NP_001155199.1:n.-107+19T>C
NM_001161728.1:c.-106-682T>C	NP_001155200.1:n.-106-682T>C
NM_001161729.1:c.-139+19T>C	NP_001155201.1:n.-139+19T>C
NM_000300.4:c.-107+19T>C	NP_000291.1:n.-107+19T>C
NM_001161727.2:c.-107+19T>C	NP_001155199.1:n.-107+19T>C
NM_001161728.2:c.-106-682T>C	NP_001155200.1:n.-106-682T>C
NM_001395463.1:c.-107+19T>C MANE Select	NP_001382392.1:n.-107+19T>C