Canonical Allele Identifier: CA356895034

Gene: PDGFRA

Linked Data

• MyVariant Identifiers: chr4:g.55152095A>T (hg19) ; chr4:g.54285928A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54285928A>T , CM000666.2:g.54285928A>T	GRCh38
NC_000004.11:g.55152095A>T , CM000666.1:g.55152095A>T	GRCh37
NC_000004.10:g.54846852A>T	NCBI36
NG_009250.1:g.61832A>T , LRG_309:g.61832A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257290.10:c.2527A>T MANE Select	ENSP00000257290.5:p.Ile843Phe
ENST00000257290.9:c.2527A>T	ENSP00000257290.5:p.Ile843Phe
ENST00000507166.5:c.1807A>T	ENSP00000423325.1:p.Ile603Phe
NM_006206.4:c.2527A>T , LRG_309t1:c.2527A>T	NP_006197.1:p.Ile843Phe
XM_005265743.1:c.2527A>T	XP_005265800.1:p.Ile843Phe
XM_006714039.2:c.2602A>T	XP_006714102.1:p.Ile868Phe
XM_011534385.1:c.2527A>T	XP_011532687.1:p.Ile843Phe
XM_011534386.1:c.2527A>T	XP_011532688.1:p.Ile843Phe
NM_001347828.1:c.2602A>T	NP_001334757.1:p.Ile868Phe
NM_001347829.1:c.2527A>T	NP_001334758.1:p.Ile843Phe
NM_001347830.1:c.2566A>T	NP_001334759.1:p.Ile856Phe
NM_006206.5:c.2527A>T	NP_006197.1:p.Ile843Phe
NM_006206.6:c.2527A>T MANE Select	NP_006197.1:p.Ile843Phe
NM_001347828.2:c.2602A>T	NP_001334757.1:p.Ile868Phe
NM_001347829.2:c.2527A>T	NP_001334758.1:p.Ile843Phe
NM_001347830.2:c.2566A>T	NP_001334759.1:p.Ile856Phe