Canonical Allele Identifier: CA2411852755
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352679C= , CM000685.2:g.1352679C= GRCh38
NC_000023.10:g.1471572C= , CM000685.1:g.1471572C= GRCh37
NC_000023.9:g.1431572C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.616+173C= MANE Select ENSP00000327890.4:n.616+173C=
ENST00000331035.9:c.616+173C= ENSP00000327890.4:n.616+173C=
ENST00000381469.7:c.382+173C= ENSP00000370878.2:n.382+173C=
ENST00000432757.6:c.382+173C= ENSP00000414867.1:n.382+173C=
XM_005274431.3:c.616+173C= XP_005274488.1:n.616+173C=
XM_005274432.1:c.613+173C= XP_005274489.1:n.613+173C=
XR_247285.3:n.649G=
XR_430488.2:n.973G=
XR_430490.2:n.648G=
XR_951269.1:n.1177G=
XR_951270.1:n.1194G=
XR_951271.1:n.1177G=
XR_951272.1:n.1181G=
XR_951273.1:n.1108G=
XR_951274.1:n.1112G=
XR_951276.1:n.1125G=
XR_951277.1:n.1177G=
XR_951278.1:n.1177G=
XR_951279.1:n.1177G=
XR_951280.1:n.1177G=
XR_951281.1:n.1177G=
XR_951282.1:n.1022G=
XR_951283.1:n.651G=
XM_005274431.5:c.616+173C= XP_005274488.1:n.616+173C=
XM_017029491.2:c.613+173C= XP_016884980.1:n.613+173C=
XR_001755748.1:n.968G=
XR_001755749.1:n.985G=
XR_001755750.1:n.968G=
XR_001755751.1:n.968G=
XR_001755752.1:n.968G=
XR_001755753.1:n.972G=
XR_001755754.1:n.968G=
XR_001755755.1:n.899G=
XR_001755756.1:n.650G=
XR_001755757.1:n.903G=
XR_001755758.1:n.916G=
XR_001755759.1:n.764G=
XR_001755760.2:n.702G=
XR_001755761.1:n.652G=
XR_001755762.1:n.648G=