Canonical Allele Identifier: CA8611496

Gene: PLCD3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45121256C>G , CM000679.2:g.45121256C>G	GRCh38
NC_000017.10:g.43198623C>G , CM000679.1:g.43198623C>G	GRCh37
NC_000017.9:g.40554149C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619929.5:c.280G>C MANE Select	ENSP00000479636.1:p.Val94Leu
ENST00000538093.1:c.88G>C	ENSP00000440378.1:p.Val30Leu
ENST00000544446.1:n.483G>C
ENST00000590644.5:c.211G>C	ENSP00000467800.1:p.Val71Leu
ENST00000619929.4:c.280G>C	ENSP00000479636.1:p.Val94Leu
NM_133373.4:c.280G>C	NP_588614.1:p.Val94Leu
XM_011524253.1:c.280G>C	XP_011522555.1:p.Val94Leu
XM_011524253.3:c.280G>C	XP_011522555.1:p.Val94Leu
XM_024450554.1:c.280G>C	XP_024306322.1:p.Val94Leu
NM_133373.5:c.280G>C MANE Select	NP_588614.1:p.Val94Leu