Canonical Allele Identifier: CA1996762745

Gene: PDGFD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103937366T= , CM000673.2:g.103937366T=	GRCh38
NC_000011.9:g.103808094T= , CM000673.1:g.103808094T=	GRCh37
NC_000011.8:g.103313304T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393158.7:c.772+6086A= MANE Select	ENSP00000376865.2:n.772+6086A=
ENST00000302251.9:c.754+6086A=	ENSP00000302193.5:n.754+6086A=
ENST00000393158.6:c.772+6086A=	ENSP00000376865.2:n.772+6086A=
NM_025208.4:c.772+6086A=	NP_079484.1:n.772+6086A=
NM_033135.3:c.754+6086A=	NP_149126.1:n.754+6086A=
NM_025208.5:c.772+6086A= MANE Select	NP_079484.1:n.772+6086A=
NM_033135.4:c.754+6086A=	NP_149126.1:n.754+6086A=