Canonical Allele Identifier: CA1505969322

Gene: PDGFC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762541G= , CM000666.2:g.156762541G=	GRCh38
NC_000004.11:g.157683693G= , CM000666.1:g.157683693G=	GRCh37
NC_000004.10:g.157903143G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.*549C= MANE Select	ENSP00000422464.1:n.*549C=
ENST00000274071.6:c.*1495C=	ENSP00000274071.2:n.*1495C=
ENST00000502773.5:c.*549C=	ENSP00000422464.1:n.*549C=
NM_016205.2:c.*549C=	NP_057289.1:n.*549C=
NR_036641.1:n.2139C=
XM_011532124.1:c.*549C=	XP_011530426.1:n.*549C=
XM_011532125.1:c.*549C=	XP_011530427.1:n.*549C=
XM_011532124.2:c.*549C=	XP_011530426.1:n.*549C=
XM_017008455.1:c.*549C=	XP_016863944.1:n.*549C=
XM_017008456.2:c.*549C=	XP_016863945.1:n.*549C=
NM_016205.3:c.*549C= MANE Select	NP_057289.1:n.*549C=
NR_036641.2:n.2544C=