Canonical Allele Identifier: CA1505969333

Gene: PDGFC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762577C= , CM000666.2:g.156762577C=	GRCh38
NC_000004.11:g.157683729C= , CM000666.1:g.157683729C=	GRCh37
NC_000004.10:g.157903179C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.*513G= MANE Select	ENSP00000422464.1:n.*513G=
ENST00000274071.6:c.*1459G=	ENSP00000274071.2:n.*1459G=
ENST00000502773.5:c.*513G=	ENSP00000422464.1:n.*513G=
NM_016205.2:c.*513G=	NP_057289.1:n.*513G=
NR_036641.1:n.2103G=
XM_011532124.1:c.*513G=	XP_011530426.1:n.*513G=
XM_011532125.1:c.*513G=	XP_011530427.1:n.*513G=
XM_011532124.2:c.*513G=	XP_011530426.1:n.*513G=
XM_017008455.1:c.*513G=	XP_016863944.1:n.*513G=
XM_017008456.2:c.*513G=	XP_016863945.1:n.*513G=
NM_016205.3:c.*513G= MANE Select	NP_057289.1:n.*513G=
NR_036641.2:n.2508G=