Canonical Allele Identifier: CA2411852579

Gene: IL3RA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352330A= , CM000685.2:g.1352330A=	GRCh38
NC_000023.10:g.1471223A= , CM000685.1:g.1471223A=	GRCh37
NC_000023.9:g.1431223A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.440A= MANE Select	ENSP00000327890.4:p.Gln147=
ENST00000331035.9:c.440A=	ENSP00000327890.4:p.Gln147=
ENST00000381469.7:c.206A=	ENSP00000370878.2:p.Gln69=
ENST00000432757.6:c.206A=	ENSP00000414867.1:p.Gln69=
XM_005274431.3:c.440A=	XP_005274488.1:p.Gln147=
XM_005274432.1:c.437A=	XP_005274489.1:p.Gln146=
XR_247285.3:n.850T=
XR_430488.2:n.1174T=
XR_430490.2:n.849T=
XR_951269.1:n.1378T=
XR_951270.1:n.1395T=
XR_951271.1:n.1446T=
XR_951272.1:n.1382T=
XR_951273.1:n.1309T=
XR_951274.1:n.1313T=
XR_951276.1:n.1326T=
XR_951277.1:n.1378T=
XR_951278.1:n.1378T=
XR_951279.1:n.1378T=
XR_951280.1:n.1378T=
XR_951281.1:n.1378T=
XR_951282.1:n.1223T=
XR_951283.1:n.852T=
XM_005274431.5:c.440A=	XP_005274488.1:p.Gln147=
XM_017029491.2:c.437A=	XP_016884980.1:p.Gln146=
XR_001755748.1:n.1169T=
XR_001755751.1:n.1169T=
XR_001755752.1:n.1169T=
XR_001755754.1:n.1169T=