Canonical Allele Identifier: CA1505986221

Gene: PDGFC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156798996C= , CM000666.2:g.156798996C=	GRCh38
NC_000004.11:g.157720148C= , CM000666.1:g.157720148C=	GRCh37
NC_000004.10:g.157939598C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.495+11841G= MANE Select	ENSP00000422464.1:n.495+11841G=
ENST00000274071.6:c.*403+11841G=	ENSP00000274071.2:n.*403+11841G=
ENST00000422544.2:c.495+11841G=	ENSP00000410048.2:n.495+11841G=
ENST00000502773.5:c.495+11841G=	ENSP00000422464.1:n.495+11841G=
ENST00000506880.5:c.149+11841G=
ENST00000511985.1:n.55+11841G=
ENST00000512711.1:n.418-26103G=
NM_016205.2:c.495+11841G=	NP_057289.1:n.495+11841G=
NR_036641.1:n.1047+11841G=
XM_011532124.1:c.462+11841G=	XP_011530426.1:n.462+11841G=
XM_011532125.1:c.426+11841G=	XP_011530427.1:n.426+11841G=
XM_011532124.2:c.462+11841G=	XP_011530426.1:n.462+11841G=
XM_017008455.1:c.390+11841G=	XP_016863944.1:n.390+11841G=
XM_017008456.2:c.495+11841G=	XP_016863945.1:n.495+11841G=
NM_016205.3:c.495+11841G= MANE Select	NP_057289.1:n.495+11841G=
NR_036641.2:n.1452+11841G=