Canonical Allele Identifier: CA397299597

Gene: PLD2

Linked Data

• MyVariant Identifiers: chr17:g.4714126G>T (hg19) ; chr17:g.4810831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4810831G>T , CM000679.2:g.4810831G>T	GRCh38
NC_000017.10:g.4714126G>T , CM000679.1:g.4714126G>T	GRCh37
NC_000017.9:g.4661094G>T	NCBI36
NG_029608.1:g.8731G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263088.11:c.890G>T MANE Select	ENSP00000263088.5:p.Arg297Leu
ENST00000263088.10:c.890G>T	ENSP00000263088.5:p.Arg297Leu
ENST00000572940.5:c.890G>T	ENSP00000459571.1:p.Arg297Leu
ENST00000575246.6:c.*538G>T	ENSP00000459304.1:n.*538G>T
ENST00000575813.5:c.25G>T
NM_001243108.1:c.890G>T	NP_001230037.1:p.Arg297Leu
NM_002663.4:c.890G>T	NP_002654.3:p.Arg297Leu
XM_005256695.2:c.890G>T	XP_005256752.1:p.Arg297Leu
XM_005256696.2:c.-317G>T	XP_005256753.1:n.-317G>T
XM_011523941.1:c.890G>T	XP_011522243.1:p.Arg297Leu
XM_011523942.1:c.890G>T	XP_011522244.1:p.Arg297Leu
XM_017024764.2:c.-317G>T	XP_016880253.1:n.-317G>T
XR_001752533.2:n.952G>T
XR_001752534.2:n.952G>T
XR_001752535.2:n.952G>T
XR_001752536.2:n.952G>T
XR_001752537.2:n.952G>T
XR_002958023.1:n.952G>T
XR_002958024.1:n.952G>T
NM_002663.5:c.890G>T MANE Select	NP_002654.3:p.Arg297Leu
NM_001243108.2:c.890G>T	NP_001230037.1:p.Arg297Leu