Canonical Allele Identifier: CA2411852575
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352322C= , CM000685.2:g.1352322C= GRCh38
NC_000023.10:g.1471215C= , CM000685.1:g.1471215C= GRCh37
NC_000023.9:g.1431215C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.432C= MANE Select ENSP00000327890.4:p.Asn144=
ENST00000331035.9:c.432C= ENSP00000327890.4:p.Asn144=
ENST00000381469.7:c.198C= ENSP00000370878.2:p.Asn66=
ENST00000432757.6:c.198C= ENSP00000414867.1:p.Asn66=
XM_005274431.3:c.432C= XP_005274488.1:p.Asn144=
XM_005274432.1:c.432-3C= XP_005274489.1:n.432-3C=
XR_247285.3:n.858G=
XR_430488.2:n.1182G=
XR_430490.2:n.857G=
XR_951269.1:n.1386G=
XR_951270.1:n.1403G=
XR_951271.1:n.1454G=
XR_951272.1:n.1390G=
XR_951273.1:n.1317G=
XR_951274.1:n.1321G=
XR_951276.1:n.1334G=
XR_951277.1:n.1386G=
XR_951278.1:n.1386G=
XR_951279.1:n.1386G=
XR_951280.1:n.1386G=
XR_951281.1:n.1386G=
XR_951282.1:n.1231G=
XR_951283.1:n.860G=
XM_005274431.5:c.432C= XP_005274488.1:p.Asn144=
XM_017029491.2:c.432-3C= XP_016884980.1:n.432-3C=
XR_001755748.1:n.1177G=
XR_001755751.1:n.1177G=
XR_001755752.1:n.1177G=
XR_001755754.1:n.1177G=