Canonical Allele Identifier: CA2161030992

Gene: PLD4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104926387T= , CM000676.2:g.104926387T=	GRCh38
NC_000014.8:g.105392724T= , CM000676.1:g.105392724T=	GRCh37
NC_000014.7:g.104463769T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392593.9:c.1-754T= MANE Select	ENSP00000376372.5:n.1-754T=
ENST00000649344.1:c.1-754T=	ENSP00000497627.1:n.1-754T=
ENST00000392593.8:c.1-754T=	ENSP00000376372.4:n.1-754T=
ENST00000472901.1:n.112-754T=
ENST00000540372.5:c.-17-716T=	ENSP00000438677.1:n.-17-716T=
ENST00000557573.1:c.1-754T=	ENSP00000451278.1:n.1-754T=
NM_001308174.1:c.-17-716T=	NP_001295103.1:n.-17-716T=
NM_138790.2:c.1-754T=	NP_620145.2:n.1-754T=
NM_138790.3:c.1-754T=	NP_620145.2:n.1-754T=
XM_011536411.1:c.-17-716T=	XP_011534713.1:n.-17-716T=
XM_011536411.2:c.-17-716T=	XP_011534713.1:n.-17-716T=
XM_017020965.1:c.1-754T=	XP_016876454.1:n.1-754T=
XM_024449469.1:c.-17-716T=	XP_024305237.1:n.-17-716T=
XM_024449470.1:c.1-754T=	XP_024305238.1:n.1-754T=
NM_001308174.2:c.-17-716T=	NP_001295103.1:n.-17-716T=
NM_138790.5:c.1-754T= MANE Select	NP_620145.2:n.1-754T=