Canonical Allele Identifier: CA2574247676

Gene: PLA2G2A

Linked Data

• gnomAD v4: 1-19978591-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978591T>C , CM000663.2:g.19978591T>C	GRCh38
NC_000001.10:g.20305084T>C , CM000663.1:g.20305084T>C	GRCh37
NC_000001.9:g.20177671T>C	NCBI36
NG_012928.1:g.6849A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-67A>G MANE Select	ENSP00000504762.1:n.41-67A>G
ENST00000400520.8:c.41-67A>G	ENSP00000383364.3:n.41-67A>G
ENST00000482011.2:c.41-67A>G	ENSP00000504762.1:n.41-67A>G
ENST00000649436.1:c.-1-107A>G	ENSP00000496912.1:n.-1-107A>G
ENST00000375111.7:c.41-67A>G	ENSP00000364252.3:n.41-67A>G
ENST00000400520.7:c.41-67A>G	ENSP00000383364.3:n.41-67A>G
ENST00000461140.1:n.335-107A>G
ENST00000469162.5:n.207-67A>G
ENST00000482011.1:n.313-67A>G
ENST00000491964.5:n.273-67A>G
ENST00000496748.1:n.324A>G
NM_000300.3:c.41-67A>G	NP_000291.1:n.41-67A>G
NM_001161727.1:c.41-67A>G	NP_001155199.1:n.41-67A>G
NM_001161728.1:c.41-67A>G	NP_001155200.1:n.41-67A>G
NM_001161729.1:c.41-67A>G	NP_001155201.1:n.41-67A>G
NM_000300.4:c.41-67A>G	NP_000291.1:n.41-67A>G
NM_001161727.2:c.41-67A>G	NP_001155199.1:n.41-67A>G
NM_001161728.2:c.41-67A>G	NP_001155200.1:n.41-67A>G
NM_001395463.1:c.41-67A>G MANE Select	NP_001382392.1:n.41-67A>G