Canonical Allele Identifier: CA2411852497
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352184C= , CM000685.2:g.1352184C= GRCh38
NC_000023.10:g.1471077C= , CM000685.1:g.1471077C= GRCh37
NC_000023.9:g.1431077C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.383C= MANE Select ENSP00000327890.4:p.Pro128=
ENST00000331035.9:c.383C= ENSP00000327890.4:p.Pro128=
ENST00000381469.7:c.149C= ENSP00000370878.2:p.Pro50=
ENST00000432757.6:c.149C= ENSP00000414867.1:p.Pro50=
XM_005274431.3:c.383C= XP_005274488.1:p.Pro128=
XM_005274432.1:c.383C= XP_005274489.1:p.Pro128=
XR_247285.3:n.870+126G=
XR_430488.2:n.1194+126G=
XR_430490.2:n.869+126G=
XR_951269.1:n.1398+126G=
XR_951270.1:n.1415+126G=
XR_951271.1:n.1466+126G=
XR_951272.1:n.1402+126G=
XR_951273.1:n.1329+126G=
XR_951274.1:n.1333+126G=
XR_951276.1:n.1346+126G=
XR_951277.1:n.1398+126G=
XR_951278.1:n.1398+126G=
XR_951279.1:n.1398+126G=
XR_951280.1:n.1398+126G=
XR_951281.1:n.1398+126G=
XR_951282.1:n.1243+126G=
XR_951283.1:n.872+126G=
XM_005274431.5:c.383C= XP_005274488.1:p.Pro128=
XM_017029491.2:c.383C= XP_016884980.1:p.Pro128=
XR_001755748.1:n.1189+126G=
XR_001755751.1:n.1189+126G=
XR_001755752.1:n.1189+126G=
XR_001755754.1:n.1189+126G=