Canonical Allele Identifier: CA1213335760

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs12746200

Genomic Alleles

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

Transcript Alleles

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