Canonical Allele Identifier: CA1996762749
Gene: PDGFD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103937369A= , CM000673.2:g.103937369A= GRCh38
NC_000011.9:g.103808097A= , CM000673.1:g.103808097A= GRCh37
NC_000011.8:g.103313307A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393158.7:c.772+6083T= MANE Select ENSP00000376865.2:n.772+6083T=
ENST00000302251.9:c.754+6083T= ENSP00000302193.5:n.754+6083T=
ENST00000393158.6:c.772+6083T= ENSP00000376865.2:n.772+6083T=
NM_025208.4:c.772+6083T= NP_079484.1:n.772+6083T=
NM_033135.3:c.754+6083T= NP_149126.1:n.754+6083T=
NM_025208.5:c.772+6083T= MANE Select NP_079484.1:n.772+6083T=
NM_033135.4:c.754+6083T= NP_149126.1:n.754+6083T=
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