Canonical Allele Identifier: CA356894847
Gene: PDGFRA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54285840G>T , CM000666.2:g.54285840G>T GRCh38
NC_000004.11:g.55152007G>T , CM000666.1:g.55152007G>T GRCh37
NC_000004.10:g.54846764G>T NCBI36
NG_009250.1:g.61744G>T , LRG_309:g.61744G>T

Transcript Alleles

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