Canonical Allele Identifier: CA2643827767

Gene: PLA2G2A

Linked Data

• gnomAD v4: 1-19978573-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978576del , CM000663.2:g.19978576del	GRCh38
NC_000001.10:g.20305069del , CM000663.1:g.20305069del	GRCh37
NC_000001.9:g.20177656del	NCBI36
NG_012928.1:g.6866del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-50del MANE Select	ENSP00000504762.1:n.41-50del
ENST00000400520.8:c.41-50del	ENSP00000383364.3:n.41-50del
ENST00000482011.2:c.41-50del	ENSP00000504762.1:n.41-50del
ENST00000649436.1:c.-1-90del	ENSP00000496912.1:n.-1-90del
ENST00000375111.7:c.41-50del	ENSP00000364252.3:n.41-50del
ENST00000400520.7:c.41-50del	ENSP00000383364.3:n.41-50del
ENST00000461140.1:n.335-90del
ENST00000469162.5:n.207-50del
ENST00000482011.1:n.313-50del
ENST00000491964.5:n.273-50del
ENST00000496748.1:n.341del
NM_000300.3:c.41-50del	NP_000291.1:n.41-50del
NM_001161727.1:c.41-50del	NP_001155199.1:n.41-50del
NM_001161728.1:c.41-50del	NP_001155200.1:n.41-50del
NM_001161729.1:c.41-50del	NP_001155201.1:n.41-50del
NM_000300.4:c.41-50del	NP_000291.1:n.41-50del
NM_001161727.2:c.41-50del	NP_001155199.1:n.41-50del
NM_001161728.2:c.41-50del	NP_001155200.1:n.41-50del
NM_001395463.1:c.41-50del MANE Select	NP_001382392.1:n.41-50del