Canonical Allele Identifier: CA399851923

Gene: PLCD3

Genomic Alleles

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

Transcript Alleles

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