Canonical Allele Identifier: CA1157334035

Gene: PLA2G2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978518_19978519delinsAG , CM000663.2:g.19978518_19978519delinsAG	GRCh38
NC_000001.10:g.20305011_20305012delinsAG , CM000663.1:g.20305011_20305012delinsAG	GRCh37
NC_000001.9:g.20177598_20177599delinsAG	NCBI36
NG_012928.1:g.6921_6922delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.46_47delinsCT MANE Select	ENSP00000504762.1:p.Leu16=
ENST00000400520.8:c.46_47delinsCT	ENSP00000383364.3:p.Leu16=
ENST00000482011.2:c.46_47delinsCT	ENSP00000504762.1:p.Leu16=
ENST00000649436.1:c.-1-35_-1-34delinsCT	ENSP00000496912.1:n.-1-35_-1-34delinsCT
ENST00000375111.7:c.46_47delinsCT	ENSP00000364252.3:p.Leu16=
ENST00000400520.7:c.46_47delinsCT	ENSP00000383364.3:p.Leu16=
ENST00000461140.1:n.335-35_335-34delinsCT
ENST00000469162.5:n.212_213delinsCT
ENST00000482011.1:n.318_319delinsCT
ENST00000491964.5:n.278_279delinsCT
ENST00000496748.1:n.396_397delinsCT
NM_000300.3:c.46_47delinsCT	NP_000291.1:p.Leu16=
NM_001161727.1:c.46_47delinsCT	NP_001155199.1:p.Leu16=
NM_001161728.1:c.46_47delinsCT	NP_001155200.1:p.Leu16=
NM_001161729.1:c.46_47delinsCT	NP_001155201.1:p.Leu16=
NM_000300.4:c.46_47delinsCT	NP_000291.1:p.Leu16=
NM_001161727.2:c.46_47delinsCT	NP_001155199.1:p.Leu16=
NM_001161728.2:c.46_47delinsCT	NP_001155200.1:p.Leu16=
NM_001395463.1:c.46_47delinsCT MANE Select	NP_001382392.1:p.Leu16=