Canonical Allele Identifier: CA2244570383

Gene: PLD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4810832G= , CM000679.2:g.4810832G=	GRCh38
NC_000017.10:g.4714127G= , CM000679.1:g.4714127G=	GRCh37
NC_000017.9:g.4661095G=	NCBI36
NG_029608.1:g.8732G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263088.11:c.891G= MANE Select	ENSP00000263088.5:p.Arg297=
ENST00000263088.10:c.891G=	ENSP00000263088.5:p.Arg297=
ENST00000572940.5:c.891G=	ENSP00000459571.1:p.Arg297=
ENST00000575246.6:c.*539G=	ENSP00000459304.1:n.*539G=
ENST00000575813.5:c.26G=
NM_001243108.1:c.891G=	NP_001230037.1:p.Arg297=
NM_002663.4:c.891G=	NP_002654.3:p.Arg297=
XM_005256695.2:c.891G=	XP_005256752.1:p.Arg297=
XM_005256696.2:c.-316G=	XP_005256753.1:n.-316G=
XM_011523941.1:c.891G=	XP_011522243.1:p.Arg297=
XM_011523942.1:c.891G=	XP_011522244.1:p.Arg297=
XM_017024764.2:c.-316G=	XP_016880253.1:n.-316G=
XR_001752533.2:n.953G=
XR_001752534.2:n.953G=
XR_001752535.2:n.953G=
XR_001752536.2:n.953G=
XR_001752537.2:n.953G=
XR_002958023.1:n.953G=
XR_002958024.1:n.953G=
NM_002663.5:c.891G= MANE Select	NP_002654.3:p.Arg297=
NM_001243108.2:c.891G=	NP_001230037.1:p.Arg297=