Canonical Allele Identifier: CA2261715049

Gene: PLCD3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45130754A= , CM000679.2:g.45130754A=	GRCh38
NC_000017.10:g.43208121A= , CM000679.1:g.43208121A=	GRCh37
NC_000017.9:g.40563647A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_133373.5:c.163+1494T= MANE Select	NP_588614.1:n.163+1494T=
ENST00000619929.5:c.163+1494T= MANE Select	ENSP00000479636.1:n.163+1494T=
NM_133373.4:c.163+1494T=	NP_588614.1:n.163+1494T=
ENST00000538093.1:c.-30+2324T=	ENSP00000440378.1:n.-30+2324T=
ENST00000544446.1:n.272-1468T=
ENST00000590644.5:c.94+2497T=	ENSP00000467800.1:n.94+2497T=
ENST00000619929.4:c.163+1494T=	ENSP00000479636.1:n.163+1494T=
XM_011524253.1:c.163+1494T=	XP_011522555.1:n.163+1494T=
XM_011524253.3:c.163+1494T=	XP_011522555.1:n.163+1494T=
XM_024450554.1:c.163+1494T=	XP_024306322.1:n.163+1494T=