Canonical Allele Identifier: CA1458529961

Gene: PDGFRA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54267542C= , CM000666.2:g.54267542C=	GRCh38
NC_000004.11:g.55133709C= , CM000666.1:g.55133709C=	GRCh37
NC_000004.10:g.54828466C=	NCBI36
NG_009250.1:g.43446C= , LRG_309:g.43446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257290.10:c.932-10C= MANE Select	ENSP00000257290.5:n.932-10C=
ENST00000257290.9:c.932-10C=	ENSP00000257290.5:n.932-10C=
ENST00000507166.5:c.1018-7383C=	ENSP00000423325.1:n.1018-7383C=
ENST00000509092.5:n.750-10C=
ENST00000509490.5:c.932-10C=	ENSP00000424218.1:n.932-10C=
NM_006206.4:c.932-10C= , LRG_309t1:c.932-10C=	NP_006197.1:n.932-10C=
XM_005265743.1:c.932-10C=	XP_005265800.1:n.932-10C=
XM_006714039.2:c.1007-10C=	XP_006714102.1:n.1007-10C=
XM_006714041.2:c.1007-10C=	XP_006714104.1:n.1007-10C=
XM_011534385.1:c.932-10C=	XP_011532687.1:n.932-10C=
XM_011534386.1:c.932-10C=	XP_011532688.1:n.932-10C=
NM_001347827.1:c.932-10C=	NP_001334756.1:n.932-10C=
NM_001347828.1:c.1007-10C=	NP_001334757.1:n.1007-10C=
NM_001347829.1:c.932-10C=	NP_001334758.1:n.932-10C=
NM_001347830.1:c.971-10C=	NP_001334759.1:n.971-10C=
NM_006206.5:c.932-10C=	NP_006197.1:n.932-10C=
XM_006714041.3:c.1007-10C=	XP_006714104.1:n.1007-10C=
XM_017008281.1:c.971-10C=	XP_016863770.1:n.971-10C=
NM_006206.6:c.932-10C= MANE Select	NP_006197.1:n.932-10C=
NM_001347827.2:c.932-10C=	NP_001334756.1:n.932-10C=
NM_001347828.2:c.1007-10C=	NP_001334757.1:n.1007-10C=
NM_001347829.2:c.932-10C=	NP_001334758.1:n.932-10C=
NM_001347830.2:c.971-10C=	NP_001334759.1:n.971-10C=