Canonical Allele Identifier: CA2705791264

Gene: PDGFRA

Linked Data

• dbSNP Id: rs765706139

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54285828C>G , CM000666.2:g.54285828C>G	GRCh38
NC_000004.11:g.55151995C>G , CM000666.1:g.55151995C>G	GRCh37
NC_000004.10:g.54846752C>G	NCBI36
NG_009250.1:g.61732C>G , LRG_309:g.61732C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257290.10:c.2440-13C>G MANE Select	ENSP00000257290.5:n.2440-13C>G
ENST00000257290.9:c.2440-13C>G	ENSP00000257290.5:n.2440-13C>G
ENST00000507166.5:c.1720-13C>G	ENSP00000423325.1:n.1720-13C>G
NM_006206.4:c.2440-13C>G , LRG_309t1:c.2440-13C>G	NP_006197.1:n.2440-13C>G
XM_005265743.1:c.2440-13C>G	XP_005265800.1:n.2440-13C>G
XM_006714039.2:c.2515-13C>G	XP_006714102.1:n.2515-13C>G
XM_011534385.1:c.2440-13C>G	XP_011532687.1:n.2440-13C>G
XM_011534386.1:c.2440-13C>G	XP_011532688.1:n.2440-13C>G
NM_001347828.1:c.2515-13C>G	NP_001334757.1:n.2515-13C>G
NM_001347829.1:c.2440-13C>G	NP_001334758.1:n.2440-13C>G
NM_001347830.1:c.2479-13C>G	NP_001334759.1:n.2479-13C>G
NM_006206.5:c.2440-13C>G	NP_006197.1:n.2440-13C>G
NM_006206.6:c.2440-13C>G MANE Select	NP_006197.1:n.2440-13C>G
NM_001347828.2:c.2515-13C>G	NP_001334757.1:n.2515-13C>G
NM_001347829.2:c.2440-13C>G	NP_001334758.1:n.2440-13C>G
NM_001347830.2:c.2479-13C>G	NP_001334759.1:n.2479-13C>G