Canonical Allele Identifier: CA2740115022

Gene: PLA2G2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978550G>A , CM000663.2:g.19978550G>A	GRCh38
NC_000001.10:g.20305043G>A , CM000663.1:g.20305043G>A	GRCh37
NC_000001.9:g.20177630G>A	NCBI36
NG_012928.1:g.6890C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-26C>T MANE Select	ENSP00000504762.1:n.41-26C>T
ENST00000400520.8:c.41-26C>T	ENSP00000383364.3:n.41-26C>T
ENST00000482011.2:c.41-26C>T	ENSP00000504762.1:n.41-26C>T
ENST00000649436.1:c.-1-66C>T	ENSP00000496912.1:n.-1-66C>T
ENST00000375111.7:c.41-26C>T	ENSP00000364252.3:n.41-26C>T
ENST00000400520.7:c.41-26C>T	ENSP00000383364.3:n.41-26C>T
ENST00000461140.1:n.335-66C>T
ENST00000469162.5:n.207-26C>T
ENST00000482011.1:n.313-26C>T
ENST00000491964.5:n.273-26C>T
ENST00000496748.1:n.365C>T
NM_000300.3:c.41-26C>T	NP_000291.1:n.41-26C>T
NM_001161727.1:c.41-26C>T	NP_001155199.1:n.41-26C>T
NM_001161728.1:c.41-26C>T	NP_001155200.1:n.41-26C>T
NM_001161729.1:c.41-26C>T	NP_001155201.1:n.41-26C>T
NM_000300.4:c.41-26C>T	NP_000291.1:n.41-26C>T
NM_001161727.2:c.41-26C>T	NP_001155199.1:n.41-26C>T
NM_001161728.2:c.41-26C>T	NP_001155200.1:n.41-26C>T
NM_001395463.1:c.41-26C>T MANE Select	NP_001382392.1:n.41-26C>T