Canonical Allele Identifier: CA356891762
Gene: PDGFRA HGNC NCBI

Linked Data

dbSNP Id: rs2110267488

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54267704G>A , CM000666.2:g.54267704G>A GRCh38
NC_000004.11:g.55133871G>A , CM000666.1:g.55133871G>A GRCh37
NC_000004.10:g.54828628G>A NCBI36
NG_009250.1:g.43608G>A , LRG_309:g.43608G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257290.10:c.1084G>A MANE Select ENSP00000257290.5:p.Glu362Lys
ENST00000257290.9:c.1084G>A ENSP00000257290.5:p.Glu362Lys
ENST00000507166.5:c.1018-7221G>A ENSP00000423325.1:n.1018-7221G>A
ENST00000509092.5:n.902G>A
ENST00000509490.5:c.1084G>A ENSP00000424218.1:p.Glu362Lys
NM_006206.4:c.1084G>A , LRG_309t1:c.1084G>A NP_006197.1:p.Glu362Lys
XM_005265743.1:c.1084G>A XP_005265800.1:p.Glu362Lys
XM_006714039.2:c.1159G>A XP_006714102.1:p.Glu387Lys
XM_006714041.2:c.1159G>A XP_006714104.1:p.Glu387Lys
XM_011534385.1:c.1084G>A XP_011532687.1:p.Glu362Lys
XM_011534386.1:c.1084G>A XP_011532688.1:p.Glu362Lys
NM_001347827.1:c.1084G>A NP_001334756.1:p.Glu362Lys
NM_001347828.1:c.1159G>A NP_001334757.1:p.Glu387Lys
NM_001347829.1:c.1084G>A NP_001334758.1:p.Glu362Lys
NM_001347830.1:c.1123G>A NP_001334759.1:p.Glu375Lys
NM_006206.5:c.1084G>A NP_006197.1:p.Glu362Lys
XM_006714041.3:c.1159G>A XP_006714104.1:p.Glu387Lys
XM_017008281.1:c.1123G>A XP_016863770.1:p.Glu375Lys
NM_006206.6:c.1084G>A MANE Select NP_006197.1:p.Glu362Lys
NM_001347827.2:c.1084G>A NP_001334756.1:p.Glu362Lys
NM_001347828.2:c.1159G>A NP_001334757.1:p.Glu387Lys
NM_001347829.2:c.1084G>A NP_001334758.1:p.Glu362Lys
NM_001347830.2:c.1123G>A NP_001334759.1:p.Glu375Lys