Canonical Allele Identifier: CA2411852750
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352671C= , CM000685.2:g.1352671C= GRCh38
NC_000023.10:g.1471564C= , CM000685.1:g.1471564C= GRCh37
NC_000023.9:g.1431564C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.616+165C= MANE Select ENSP00000327890.4:n.616+165C=
ENST00000331035.9:c.616+165C= ENSP00000327890.4:n.616+165C=
ENST00000381469.7:c.382+165C= ENSP00000370878.2:n.382+165C=
ENST00000432757.6:c.382+165C= ENSP00000414867.1:n.382+165C=
XM_005274431.3:c.616+165C= XP_005274488.1:n.616+165C=
XM_005274432.1:c.613+165C= XP_005274489.1:n.613+165C=
XR_247285.3:n.657G=
XR_430488.2:n.981G=
XR_430490.2:n.656G=
XR_951269.1:n.1185G=
XR_951270.1:n.1202G=
XR_951271.1:n.1185G=
XR_951272.1:n.1189G=
XR_951273.1:n.1116G=
XR_951274.1:n.1120G=
XR_951276.1:n.1133G=
XR_951277.1:n.1185G=
XR_951278.1:n.1185G=
XR_951279.1:n.1185G=
XR_951280.1:n.1185G=
XR_951281.1:n.1185G=
XR_951282.1:n.1030G=
XR_951283.1:n.659G=
XM_005274431.5:c.616+165C= XP_005274488.1:n.616+165C=
XM_017029491.2:c.613+165C= XP_016884980.1:n.613+165C=
XR_001755748.1:n.976G=
XR_001755749.1:n.993G=
XR_001755750.1:n.976G=
XR_001755751.1:n.976G=
XR_001755752.1:n.976G=
XR_001755753.1:n.980G=
XR_001755754.1:n.976G=
XR_001755755.1:n.907G=
XR_001755756.1:n.658G=
XR_001755757.1:n.911G=
XR_001755758.1:n.924G=
XR_001755759.1:n.772G=
XR_001755760.2:n.710G=
XR_001755761.1:n.660G=
XR_001755762.1:n.656G=