Canonical Allele Identifier: CA439287225

Gene: PDGFRA

Linked Data

• ClinVar Variation Id: 1088330
• ClinVar RCV Id: RCV001406744
• dbSNP Id: rs2110300729
• gnomAD v4: 4-54274960-T-C
• MyVariant Identifiers: chr4:g.55141127T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54274960T>C , CM000666.2:g.54274960T>C	GRCh38
NC_000004.11:g.55141127T>C , CM000666.1:g.55141127T>C	GRCh37
NC_000004.10:g.54835884T>C	NCBI36
NG_009250.1:g.50864T>C , LRG_309:g.50864T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257290.10:c.1773T>C MANE Select	ENSP00000257290.5:p.Asp591=
ENST00000257290.9:c.1773T>C	ENSP00000257290.5:p.Asp591=
ENST00000507166.5:c.1053T>C	ENSP00000423325.1:p.Asp351=
ENST00000509092.5:n.1591T>C
ENST00000509490.5:c.1773T>C	ENSP00000424218.1:p.Asp591=
NM_006206.4:c.1773T>C , LRG_309t1:c.1773T>C	NP_006197.1:p.Asp591=
XM_005265743.1:c.1773T>C	XP_005265800.1:p.Asp591=
XM_006714039.2:c.1848T>C	XP_006714102.1:p.Asp616=
XM_006714041.2:c.1848T>C	XP_006714104.1:p.Asp616=
XM_011534385.1:c.1773T>C	XP_011532687.1:p.Asp591=
XM_011534386.1:c.1773T>C	XP_011532688.1:p.Asp591=
NM_001347827.1:c.1773T>C	NP_001334756.1:p.Asp591=
NM_001347828.1:c.1848T>C	NP_001334757.1:p.Asp616=
NM_001347829.1:c.1773T>C	NP_001334758.1:p.Asp591=
NM_001347830.1:c.1812T>C	NP_001334759.1:p.Asp604=
NM_006206.5:c.1773T>C	NP_006197.1:p.Asp591=
XM_006714041.3:c.1848T>C	XP_006714104.1:p.Asp616=
XM_017008281.1:c.1812T>C	XP_016863770.1:p.Asp604=
NM_006206.6:c.1773T>C MANE Select	NP_006197.1:p.Asp591=
NM_001347827.2:c.1773T>C	NP_001334756.1:p.Asp591=
NM_001347828.2:c.1848T>C	NP_001334757.1:p.Asp616=
NM_001347829.2:c.1773T>C	NP_001334758.1:p.Asp591=
NM_001347830.2:c.1812T>C	NP_001334759.1:p.Asp604=