Canonical Allele Identifier: CA915941899

Gene: PLCD1

Linked Data

• ClinVar Variation Id: 733776
• ClinVar RCV Id: RCV000909125
• dbSNP Id: rs1575345323

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38008641A>G , CM000665.2:g.38008641A>G	GRCh38
NC_000003.11:g.38050132A>G , CM000665.1:g.38050132A>G	GRCh37
NC_000003.10:g.38025136A>G	NCBI36
NG_031922.1:g.26023T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334661.5:c.1724-5T>C MANE Select	ENSP00000335600.4:n.1724-5T>C
ENST00000334661.4:c.1724-5T>C	ENSP00000335600.4:n.1724-5T>C
ENST00000461445.5:n.2442T>C
ENST00000463876.5:c.1787-5T>C	ENSP00000430344.1:n.1787-5T>C
ENST00000484829.5:n.871-5T>C
ENST00000495367.1:n.509-5T>C
ENST00000495395.1:n.124T>C
NM_001130964.1:c.1787-5T>C	NP_001124436.1:n.1787-5T>C
NM_006225.3:c.1724-5T>C	NP_006216.2:n.1724-5T>C
NR_024071.1:n.2218-5T>C
XM_017006622.1:c.1550-5T>C	XP_016862111.1:n.1550-5T>C
XR_001740173.2:n.1930-274T>C
NM_001130964.2:c.1787-5T>C	NP_001124436.1:n.1787-5T>C
NM_006225.4:c.1724-5T>C MANE Select	NP_006216.2:n.1724-5T>C
NR_024071.2:n.1951-5T>C