Canonical Allele Identifier: CA96866772
Gene: PDGFRA HGNC NCBI

Linked Data

dbSNP Id: rs121913257
COSMIC: COSM12408

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54285927_54285939delinsG , CM000666.2:g.54285927_54285939delinsG GRCh38
NC_000004.11:g.55152094_55152106delinsG , CM000666.1:g.55152094_55152106delinsG GRCh37
NC_000004.10:g.54846851_54846863delinsG NCBI36
NG_009250.1:g.61831_61843delinsG , LRG_309:g.61831_61843delinsG

Transcript Alleles

HGVS Amino-acid Change
ENST00000257290.10:c.2526_2538delinsG MANE Select ENSP00000257290.5:p.Asp842_Asp846delinsGlu
ENST00000257290.9:c.2526_2538delinsG ENSP00000257290.5:p.Asp842_Asp846delinsGlu
ENST00000507166.5:c.1806_1818delinsG ENSP00000423325.1:p.Asp602_Asp606delinsGlu
NM_006206.4:c.2526_2538delinsG , LRG_309t1:c.2526_2538delinsG NP_006197.1:p.Asp842_Asp846delinsGlu
XM_005265743.1:c.2526_2538delinsG XP_005265800.1:p.Asp842_Asp846delinsGlu
XM_006714039.2:c.2601_2613delinsG XP_006714102.1:p.Asp867_Asp871delinsGlu
XM_011534385.1:c.2526_2538delinsG XP_011532687.1:p.Asp842_Asp846delinsGlu
XM_011534386.1:c.2526_2538delinsG XP_011532688.1:p.Asp842_Asp846delinsGlu
NM_001347828.1:c.2601_2613delinsG NP_001334757.1:p.Asp867_Asp871delinsGlu
NM_001347829.1:c.2526_2538delinsG NP_001334758.1:p.Asp842_Asp846delinsGlu
NM_001347830.1:c.2565_2577delinsG NP_001334759.1:p.Asp855_Asp859delinsGlu
NM_006206.5:c.2526_2538delinsG NP_006197.1:p.Asp842_Asp846delinsGlu
NM_006206.6:c.2526_2538delinsG MANE Select NP_006197.1:p.Asp842_Asp846delinsGlu
NM_001347828.2:c.2601_2613delinsG NP_001334757.1:p.Asp867_Asp871delinsGlu
NM_001347829.2:c.2526_2538delinsG NP_001334758.1:p.Asp842_Asp846delinsGlu
NM_001347830.2:c.2565_2577delinsG NP_001334759.1:p.Asp855_Asp859delinsGlu