Canonical Allele Identifier: CA397299635

Gene: PLD2

Linked Data

• MyVariant Identifiers: chr17:g.4714135G>C (hg19) ; chr17:g.4810840G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4810840G>C , CM000679.2:g.4810840G>C	GRCh38
NC_000017.10:g.4714135G>C , CM000679.1:g.4714135G>C	GRCh37
NC_000017.9:g.4661103G>C	NCBI36
NG_029608.1:g.8740G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263088.11:c.899G>C MANE Select	ENSP00000263088.5:p.Arg300Pro
ENST00000263088.10:c.899G>C	ENSP00000263088.5:p.Arg300Pro
ENST00000572940.5:c.899G>C	ENSP00000459571.1:p.Arg300Pro
ENST00000575246.6:c.*547G>C	ENSP00000459304.1:n.*547G>C
ENST00000575813.5:c.34G>C
NM_001243108.1:c.899G>C	NP_001230037.1:p.Arg300Pro
NM_002663.4:c.899G>C	NP_002654.3:p.Arg300Pro
XM_005256695.2:c.899G>C	XP_005256752.1:p.Arg300Pro
XM_005256696.2:c.-308G>C	XP_005256753.1:n.-308G>C
XM_011523941.1:c.899G>C	XP_011522243.1:p.Arg300Pro
XM_011523942.1:c.899G>C	XP_011522244.1:p.Arg300Pro
XM_017024764.2:c.-308G>C	XP_016880253.1:n.-308G>C
XR_001752533.2:n.961G>C
XR_001752534.2:n.961G>C
XR_001752535.2:n.961G>C
XR_001752536.2:n.961G>C
XR_001752537.2:n.961G>C
XR_002958023.1:n.961G>C
XR_002958024.1:n.961G>C
NM_002663.5:c.899G>C MANE Select	NP_002654.3:p.Arg300Pro
NM_001243108.2:c.899G>C	NP_001230037.1:p.Arg300Pro