Canonical Allele Identifier: CA397299627

Gene: PLD2

Linked Data

• dbSNP Id: rs1597323174
• MyVariant Identifiers: chr17:g.4714132C>G (hg19) ; chr17:g.4810837C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4810837C>G , CM000679.2:g.4810837C>G	GRCh38
NC_000017.10:g.4714132C>G , CM000679.1:g.4714132C>G	GRCh37
NC_000017.9:g.4661100C>G	NCBI36
NG_029608.1:g.8737C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263088.11:c.896C>G MANE Select	ENSP00000263088.5:p.Ala299Gly
ENST00000263088.10:c.896C>G	ENSP00000263088.5:p.Ala299Gly
ENST00000572940.5:c.896C>G	ENSP00000459571.1:p.Ala299Gly
ENST00000575246.6:c.*544C>G	ENSP00000459304.1:n.*544C>G
ENST00000575813.5:c.31C>G
NM_001243108.1:c.896C>G	NP_001230037.1:p.Ala299Gly
NM_002663.4:c.896C>G	NP_002654.3:p.Ala299Gly
XM_005256695.2:c.896C>G	XP_005256752.1:p.Ala299Gly
XM_005256696.2:c.-311C>G	XP_005256753.1:n.-311C>G
XM_011523941.1:c.896C>G	XP_011522243.1:p.Ala299Gly
XM_011523942.1:c.896C>G	XP_011522244.1:p.Ala299Gly
XM_017024764.2:c.-311C>G	XP_016880253.1:n.-311C>G
XR_001752533.2:n.958C>G
XR_001752534.2:n.958C>G
XR_001752535.2:n.958C>G
XR_001752536.2:n.958C>G
XR_001752537.2:n.958C>G
XR_002958023.1:n.958C>G
XR_002958024.1:n.958C>G
NM_002663.5:c.896C>G MANE Select	NP_002654.3:p.Ala299Gly
NM_001243108.2:c.896C>G	NP_001230037.1:p.Ala299Gly