Canonical Allele Identifier: CA2411852740
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352649C= , CM000685.2:g.1352649C= GRCh38
NC_000023.10:g.1471542C= , CM000685.1:g.1471542C= GRCh37
NC_000023.9:g.1431542C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.616+143C= MANE Select ENSP00000327890.4:n.616+143C=
ENST00000331035.9:c.616+143C= ENSP00000327890.4:n.616+143C=
ENST00000381469.7:c.382+143C= ENSP00000370878.2:n.382+143C=
ENST00000432757.6:c.382+143C= ENSP00000414867.1:n.382+143C=
XM_005274431.3:c.616+143C= XP_005274488.1:n.616+143C=
XM_005274432.1:c.613+143C= XP_005274489.1:n.613+143C=
XR_247285.3:n.679G=
XR_430488.2:n.1003G=
XR_430490.2:n.678G=
XR_951269.1:n.1207G=
XR_951270.1:n.1224G=
XR_951271.1:n.1207G=
XR_951272.1:n.1211G=
XR_951273.1:n.1138G=
XR_951274.1:n.1142G=
XR_951276.1:n.1155G=
XR_951277.1:n.1207G=
XR_951278.1:n.1207G=
XR_951279.1:n.1207G=
XR_951280.1:n.1207G=
XR_951281.1:n.1207G=
XR_951282.1:n.1052G=
XR_951283.1:n.681G=
XM_005274431.5:c.616+143C= XP_005274488.1:n.616+143C=
XM_017029491.2:c.613+143C= XP_016884980.1:n.613+143C=
XR_001755748.1:n.998G=
XR_001755749.1:n.1015G=
XR_001755750.1:n.998G=
XR_001755751.1:n.998G=
XR_001755752.1:n.998G=
XR_001755753.1:n.1002G=
XR_001755754.1:n.998G=
XR_001755755.1:n.929G=
XR_001755756.1:n.680G=
XR_001755757.1:n.933G=
XR_001755758.1:n.946G=
XR_001755759.1:n.794G=
XR_001755760.2:n.732G=
XR_001755761.1:n.682G=
XR_001755762.1:n.678G=