Canonical Allele Identifier: CA2764165531

Gene: PDGFC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762469C>A , CM000666.2:g.156762469C>A	GRCh38
NC_000004.11:g.157683621C>A , CM000666.1:g.157683621C>A	GRCh37
NC_000004.10:g.157903071C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*621G>T MANE Select	ENSP00000422464.1:n.*621G>T
ENST00000274071.6:c.*1567G>T	ENSP00000274071.2:n.*1567G>T
ENST00000502773.5:c.*621G>T	ENSP00000422464.1:n.*621G>T
NM_016205.2:c.*621G>T	NP_057289.1:n.*621G>T
NR_036641.1:n.2211G>T
XM_011532124.1:c.*621G>T	XP_011530426.1:n.*621G>T
XM_011532125.1:c.*621G>T	XP_011530427.1:n.*621G>T
XM_011532124.2:c.*621G>T	XP_011530426.1:n.*621G>T
XM_017008455.1:c.*621G>T	XP_016863944.1:n.*621G>T
XM_017008456.2:c.*621G>T	XP_016863945.1:n.*621G>T
NM_016205.3:c.*621G>T MANE Select	NP_057289.1:n.*621G>T
NR_036641.2:n.2616G>T