Canonical Allele Identifier: CA2531132234
Gene: PDGFC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156762439G>A , CM000666.2:g.156762439G>A GRCh38
NC_000004.11:g.157683591G>A , CM000666.1:g.157683591G>A GRCh37
NC_000004.10:g.157903041G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.*651C>T MANE Select ENSP00000422464.1:n.*651C>T
ENST00000274071.6:c.*1597C>T ENSP00000274071.2:n.*1597C>T
ENST00000502773.5:c.*651C>T ENSP00000422464.1:n.*651C>T
NM_016205.2:c.*651C>T NP_057289.1:n.*651C>T
NR_036641.1:n.2241C>T
XM_011532124.1:c.*651C>T XP_011530426.1:n.*651C>T
XM_011532125.1:c.*651C>T XP_011530427.1:n.*651C>T
XM_011532124.2:c.*651C>T XP_011530426.1:n.*651C>T
XM_017008455.1:c.*651C>T XP_016863944.1:n.*651C>T
XM_017008456.2:c.*651C>T XP_016863945.1:n.*651C>T
NM_016205.3:c.*651C>T MANE Select NP_057289.1:n.*651C>T
NR_036641.2:n.2646C>T