Canonical Allele Identifier: CA1590817236

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155773_150155774delinsTC , CM000667.2:g.150155773_150155774delinsTC	GRCh38
NC_000005.9:g.149535336_149535337delinsTC , CM000667.1:g.149535336_149535337delinsTC	GRCh37
NC_000005.8:g.149515529_149515530delinsTC	NCBI36
NG_023367.1:g.5086_5087delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-384_-383delinsGA MANE Select	ENSP00000261799.4:n.-384_-383delinsGA
ENST00000261799.8:c.-384_-383delinsGA	ENSP00000261799.4:n.-384_-383delinsGA
ENST00000517660.1:n.87_88delinsGA
ENST00000520579.5:c.-384_-383delinsGA	ENSP00000430026.1:n.-384_-383delinsGA
ENST00000523456.1:n.99_100delinsGA
NM_002609.3:c.-384_-383delinsGA	NP_002600.1:n.-384_-383delinsGA
XM_005268464.2:c.-530_-529delinsGA	XP_005268521.1:n.-530_-529delinsGA
XM_011537659.1:c.-851_-850delinsGA	XP_011535961.1:n.-851_-850delinsGA
NM_001355016.1:c.-530_-529delinsGA	NP_001341945.1:n.-530_-529delinsGA
NM_001355017.1:c.-901_-900delinsGA	NP_001341946.1:n.-901_-900delinsGA
NR_149150.1:n.86_87delinsGA
NM_002609.4:c.-384_-383delinsGA MANE Select	NP_002600.1:n.-384_-383delinsGA
NM_001355016.2:c.-530_-529delinsGA	NP_001341945.1:n.-530_-529delinsGA
NM_001355017.2:c.-901_-900delinsGA	NP_001341946.1:n.-901_-900delinsGA
NR_149150.2:n.72_73delinsGA