Canonical Allele Identifier: CA412245819
Gene: IL3RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352329C>G , CM000685.2:g.1352329C>G GRCh38
NC_000023.10:g.1471222C>G , CM000685.1:g.1471222C>G GRCh37
NC_000023.9:g.1431222C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.439C>G MANE Select ENSP00000327890.4:p.Gln147Glu
ENST00000331035.9:c.439C>G ENSP00000327890.4:p.Gln147Glu
ENST00000381469.7:c.205C>G ENSP00000370878.2:p.Gln69Glu
ENST00000432757.6:c.205C>G ENSP00000414867.1:p.Gln69Glu
XM_005274431.3:c.439C>G XP_005274488.1:p.Gln147Glu
XM_005274432.1:c.436C>G XP_005274489.1:p.Gln146Glu
XR_247285.3:n.851G>C
XR_430488.2:n.1175G>C
XR_430490.2:n.850G>C
XR_951269.1:n.1379G>C
XR_951270.1:n.1396G>C
XR_951271.1:n.1447G>C
XR_951272.1:n.1383G>C
XR_951273.1:n.1310G>C
XR_951274.1:n.1314G>C
XR_951276.1:n.1327G>C
XR_951277.1:n.1379G>C
XR_951278.1:n.1379G>C
XR_951279.1:n.1379G>C
XR_951280.1:n.1379G>C
XR_951281.1:n.1379G>C
XR_951282.1:n.1224G>C
XR_951283.1:n.853G>C
XM_005274431.5:c.439C>G XP_005274488.1:p.Gln147Glu
XM_017029491.2:c.436C>G XP_016884980.1:p.Gln146Glu
XR_001755748.1:n.1170G>C
XR_001755751.1:n.1170G>C
XR_001755752.1:n.1170G>C
XR_001755754.1:n.1170G>C