Canonical Allele Identifier: CA1140427214

Gene: PLA2G4A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186880054A= , CM000663.2:g.186880054A=	GRCh38
NC_000001.10:g.186849186A= , CM000663.1:g.186849186A=	GRCh37
NC_000001.9:g.185115809A=	NCBI36
NG_012203.1:g.56155A=
NG_012203.2:g.56155A=

Transcript Alleles

HGVS	Amino-acid Change
NM_024420.3:c.115+9538A= MANE Select	NP_077734.2:n.115+9538A=
ENST00000367466.4:c.115+9538A= MANE Select	ENSP00000356436.3:n.115+9538A=
NM_001311193.1:c.115+9538A=	NP_001298122.1:n.115+9538A=
NM_001311193.2:c.115+9538A=	NP_001298122.2:n.115+9538A=
NM_024420.2:c.115+9538A=	NP_077734.1:n.115+9538A=
ENST00000367466.3:c.115+9538A=	ENSP00000356436.3:n.115+9538A=
ENST00000466600.1:n.184+9538A=
XM_005245267.2:c.4+9310A=	XP_005245324.1:n.4+9310A=
XM_005245267.4:c.130+9310A=	XP_005245324.2:n.130+9310A=
XM_011509641.1:c.136+9538A=	XP_011507943.1:n.136+9538A=
XM_011509642.1:c.115+9538A=	XP_011507944.1:n.115+9538A=
XM_011509642.2:c.115+9538A=	XP_011507944.1:n.115+9538A=
XM_011509643.1:c.115+9538A=	XP_011507945.1:n.115+9538A=
XR_921838.1:n.176+9538A=