Canonical Allele Identifier: CA352109664

Gene: PLCD1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38008524G>C , CM000665.2:g.38008524G>C	GRCh38
NC_000003.11:g.38050015G>C , CM000665.1:g.38050015G>C	GRCh37
NC_000003.10:g.38025019G>C	NCBI36
NG_031922.1:g.26140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334661.5:c.1836C>G MANE Select	ENSP00000335600.4:p.Asn612Lys
ENST00000334661.4:c.1836C>G	ENSP00000335600.4:p.Asn612Lys
ENST00000461445.5:n.2559C>G
ENST00000463876.5:c.1899C>G	ENSP00000430344.1:p.Asn633Lys
ENST00000484829.5:n.983C>G
ENST00000495395.1:n.241C>G
NM_001130964.1:c.1899C>G	NP_001124436.1:p.Asn633Lys
NM_006225.3:c.1836C>G	NP_006216.2:p.Asn612Lys
NR_024071.1:n.2330C>G
XM_017006622.1:c.1662C>G	XP_016862111.1:p.Asn554Lys
XR_001740173.2:n.1930-157C>G
NM_001130964.2:c.1899C>G	NP_001124436.1:p.Asn633Lys
NM_006225.4:c.1836C>G MANE Select	NP_006216.2:p.Asn612Lys
NR_024071.2:n.2063C>G