Canonical Allele Identifier: CA1157334012

Gene: PLA2G2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978512G= , CM000663.2:g.19978512G=	GRCh38
NC_000001.10:g.20305005G= , CM000663.1:g.20305005G=	GRCh37
NC_000001.9:g.20177592G=	NCBI36
NG_012928.1:g.6928C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.53C= MANE Select	ENSP00000504762.1:p.Ala18=
ENST00000400520.8:c.53C=	ENSP00000383364.3:p.Ala18=
ENST00000482011.2:c.53C=	ENSP00000504762.1:p.Ala18=
ENST00000649436.1:c.-1-28C=	ENSP00000496912.1:n.-1-28C=
ENST00000375111.7:c.53C=	ENSP00000364252.3:p.Ala18=
ENST00000400520.7:c.53C=	ENSP00000383364.3:p.Ala18=
ENST00000461140.1:n.335-28C=
ENST00000469162.5:n.219C=
ENST00000482011.1:n.325C=
ENST00000491964.5:n.285C=
ENST00000496748.1:n.403C=
NM_000300.3:c.53C=	NP_000291.1:p.Ala18=
NM_001161727.1:c.53C=	NP_001155199.1:p.Ala18=
NM_001161728.1:c.53C=	NP_001155200.1:p.Ala18=
NM_001161729.1:c.53C=	NP_001155201.1:p.Ala18=
NM_000300.4:c.53C=	NP_000291.1:p.Ala18=
NM_001161727.2:c.53C=	NP_001155199.1:p.Ala18=
NM_001161728.2:c.53C=	NP_001155200.1:p.Ala18=
NM_001395463.1:c.53C= MANE Select	NP_001382392.1:p.Ala18=