Canonical Allele Identifier: CA2764165537
Gene: PDGFC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156762555A>T , CM000666.2:g.156762555A>T GRCh38
NC_000004.11:g.157683707A>T , CM000666.1:g.157683707A>T GRCh37
NC_000004.10:g.157903157A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502773.6:c.*535T>A MANE Select ENSP00000422464.1:n.*535T>A
ENST00000274071.6:c.*1481T>A ENSP00000274071.2:n.*1481T>A
ENST00000502773.5:c.*535T>A ENSP00000422464.1:n.*535T>A
NM_016205.2:c.*535T>A NP_057289.1:n.*535T>A
NR_036641.1:n.2125T>A
XM_011532124.1:c.*535T>A XP_011530426.1:n.*535T>A
XM_011532125.1:c.*535T>A XP_011530427.1:n.*535T>A
XM_011532124.2:c.*535T>A XP_011530426.1:n.*535T>A
XM_017008455.1:c.*535T>A XP_016863944.1:n.*535T>A
XM_017008456.2:c.*535T>A XP_016863945.1:n.*535T>A
NM_016205.3:c.*535T>A MANE Select NP_057289.1:n.*535T>A
NR_036641.2:n.2530T>A
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