Canonical Allele Identifier: CA1506068202
Gene: PDGFC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971765_156971768delinsACCT , CM000666.2:g.156971765_156971768delinsACCT GRCh38
NC_000004.11:g.157892917_157892920delinsACCT , CM000666.1:g.157892917_157892920delinsACCT GRCh37
NC_000004.10:g.158112367_158112370delinsACCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-865_-862delinsAGGT MANE Select ENSP00000422464.1:n.-865_-862delinsAGGT
NM_016205.3:c.-865_-862delinsAGGT MANE Select NP_057289.1:n.-865_-862delinsAGGT
NR_036641.2:n.32_35delinsAGGT