Canonical Allele Identifier: CA2764165538
Gene: PDGFC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156762561_156762570del , CM000666.2:g.156762561_156762570del GRCh38
NC_000004.11:g.157683713_157683722del , CM000666.1:g.157683713_157683722del GRCh37
NC_000004.10:g.157903163_157903172del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.*520_*529del MANE Select ENSP00000422464.1:n.*520_*529del
ENST00000274071.6:c.*1466_*1475del ENSP00000274071.2:n.*1466_*1475del
ENST00000502773.5:c.*520_*529del ENSP00000422464.1:n.*520_*529del
NM_016205.2:c.*520_*529del NP_057289.1:n.*520_*529del
NR_036641.1:n.2110_2119del
XM_011532124.1:c.*520_*529del XP_011530426.1:n.*520_*529del
XM_011532125.1:c.*520_*529del XP_011530427.1:n.*520_*529del
XM_011532124.2:c.*520_*529del XP_011530426.1:n.*520_*529del
XM_017008455.1:c.*520_*529del XP_016863944.1:n.*520_*529del
XM_017008456.2:c.*520_*529del XP_016863945.1:n.*520_*529del
NM_016205.3:c.*520_*529del MANE Select NP_057289.1:n.*520_*529del
NR_036641.2:n.2515_2524del