Canonical Allele Identifier: CA2411852585

Gene: IL3RA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352343T= , CM000685.2:g.1352343T=	GRCh38
NC_000023.10:g.1471236T= , CM000685.1:g.1471236T=	GRCh37
NC_000023.9:g.1431236T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.453T= MANE Select	ENSP00000327890.4:p.Cys151=
ENST00000331035.9:c.453T=	ENSP00000327890.4:p.Cys151=
ENST00000381469.7:c.219T=	ENSP00000370878.2:p.Cys73=
ENST00000432757.6:c.219T=	ENSP00000414867.1:p.Cys73=
XM_005274431.3:c.453T=	XP_005274488.1:p.Cys151=
XM_005274432.1:c.450T=	XP_005274489.1:p.Cys150=
XR_247285.3:n.837A=
XR_430488.2:n.1161A=
XR_430490.2:n.836A=
XR_951269.1:n.1365A=
XR_951270.1:n.1382A=
XR_951271.1:n.1433A=
XR_951272.1:n.1369A=
XR_951273.1:n.1296A=
XR_951274.1:n.1300A=
XR_951276.1:n.1313A=
XR_951277.1:n.1365A=
XR_951278.1:n.1365A=
XR_951279.1:n.1365A=
XR_951280.1:n.1365A=
XR_951281.1:n.1365A=
XR_951282.1:n.1210A=
XR_951283.1:n.839A=
XM_005274431.5:c.453T=	XP_005274488.1:p.Cys151=
XM_017029491.2:c.450T=	XP_016884980.1:p.Cys150=
XR_001755748.1:n.1156A=
XR_001755751.1:n.1156A=
XR_001755752.1:n.1156A=
XR_001755754.1:n.1156A=