Canonical Allele Identifier: CA1505969336

Gene: PDGFC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762585T= , CM000666.2:g.156762585T=	GRCh38
NC_000004.11:g.157683737T= , CM000666.1:g.157683737T=	GRCh37
NC_000004.10:g.157903187T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*505A= MANE Select	ENSP00000422464.1:n.*505A=
ENST00000274071.6:c.*1451A=	ENSP00000274071.2:n.*1451A=
ENST00000502773.5:c.*505A=	ENSP00000422464.1:n.*505A=
NM_016205.2:c.*505A=	NP_057289.1:n.*505A=
NR_036641.1:n.2095A=
XM_011532124.1:c.*505A=	XP_011530426.1:n.*505A=
XM_011532125.1:c.*505A=	XP_011530427.1:n.*505A=
XM_011532124.2:c.*505A=	XP_011530426.1:n.*505A=
XM_017008455.1:c.*505A=	XP_016863944.1:n.*505A=
XM_017008456.2:c.*505A=	XP_016863945.1:n.*505A=
NM_016205.3:c.*505A= MANE Select	NP_057289.1:n.*505A=
NR_036641.2:n.2500A=