Canonical Allele Identifier: CA1157335465

Gene: PLA2G2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19979587A= , CM000663.2:g.19979587A=	GRCh38
NC_000001.10:g.20306080A= , CM000663.1:g.20306080A=	GRCh37
NC_000001.9:g.20178667A=	NCBI36
NG_012928.1:g.5853T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.-114T= MANE Select	ENSP00000504762.1:n.-114T=
ENST00000400520.8:c.-146T=	ENSP00000383364.3:n.-146T=
ENST00000482011.2:c.-114T=	ENSP00000504762.1:n.-114T=
ENST00000649436.1:c.-155T=	ENSP00000496912.1:n.-155T=
ENST00000375111.7:c.-114T=	ENSP00000364252.3:n.-114T=
ENST00000400520.7:c.-114T=	ENSP00000383364.3:n.-114T=
ENST00000469162.5:n.21T=
ENST00000482011.1:n.159T=
ENST00000491964.5:n.119T=
ENST00000496748.1:n.28T=
NM_000300.3:c.-114T=	NP_000291.1:n.-114T=
NM_001161727.1:c.-114T=	NP_001155199.1:n.-114T=
NM_001161728.1:c.-106-708T=	NP_001155200.1:n.-106-708T=
NM_001161729.1:c.-146T=	NP_001155201.1:n.-146T=
NM_000300.4:c.-114T=	NP_000291.1:n.-114T=
NM_001161727.2:c.-114T=	NP_001155199.1:n.-114T=
NM_001161728.2:c.-106-708T=	NP_001155200.1:n.-106-708T=
NM_001395463.1:c.-114T= MANE Select	NP_001382392.1:n.-114T=