Canonical Allele Identifier: CA1626051259

Gene: PLA2G7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.46714342A= , CM000668.2:g.46714342A=	GRCh38
NC_000006.11:g.46682079A= , CM000668.1:g.46682079A=	GRCh37
NC_000006.10:g.46790038A=	NCBI36
NG_016204.1:g.26352T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274793.12:c.470+118T= MANE Select	ENSP00000274793.7:n.470+118T=
ENST00000274793.11:c.470+118T=	ENSP00000274793.7:n.470+118T=
ENST00000537365.1:c.470+118T=	ENSP00000445666.1:n.470+118T=
NM_001168357.1:c.470+118T=	NP_001161829.1:n.470+118T=
NM_005084.3:c.470+118T=	NP_005075.3:n.470+118T=
XM_005249408.3:c.470+118T=	XP_005249465.1:n.470+118T=
XM_005249409.2:c.470+118T=	XP_005249466.1:n.470+118T=
XM_005249408.4:c.470+118T=	XP_005249465.1:n.470+118T=
XR_001743639.2:n.716+118T=
XR_002956305.1:n.515+118T=
NM_005084.4:c.470+118T= MANE Select	NP_005075.3:n.470+118T=
NM_001168357.2:c.470+118T=	NP_001161829.1:n.470+118T=