Canonical Allele Identifier: CA356894882
Gene: PDGFRA HGNC NCBI

Linked Data

COSMIC: COSM217313

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54285856C>A , CM000666.2:g.54285856C>A GRCh38
NC_000004.11:g.55152023C>A , CM000666.1:g.55152023C>A GRCh37
NC_000004.10:g.54846780C>A NCBI36
NG_009250.1:g.61760C>A , LRG_309:g.61760C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257290.10:c.2455C>A MANE Select ENSP00000257290.5:p.Leu819Met
ENST00000257290.9:c.2455C>A ENSP00000257290.5:p.Leu819Met
ENST00000507166.5:c.1735C>A ENSP00000423325.1:p.Leu579Met
NM_006206.4:c.2455C>A , LRG_309t1:c.2455C>A NP_006197.1:p.Leu819Met
XM_005265743.1:c.2455C>A XP_005265800.1:p.Leu819Met
XM_006714039.2:c.2530C>A XP_006714102.1:p.Leu844Met
XM_011534385.1:c.2455C>A XP_011532687.1:p.Leu819Met
XM_011534386.1:c.2455C>A XP_011532688.1:p.Leu819Met
NM_001347828.1:c.2530C>A NP_001334757.1:p.Leu844Met
NM_001347829.1:c.2455C>A NP_001334758.1:p.Leu819Met
NM_001347830.1:c.2494C>A NP_001334759.1:p.Leu832Met
NM_006206.5:c.2455C>A NP_006197.1:p.Leu819Met
NM_006206.6:c.2455C>A MANE Select NP_006197.1:p.Leu819Met
NM_001347828.2:c.2530C>A NP_001334757.1:p.Leu844Met
NM_001347829.2:c.2455C>A NP_001334758.1:p.Leu819Met
NM_001347830.2:c.2494C>A NP_001334759.1:p.Leu832Met