Canonical Allele Identifier: CA412245580
Gene: IL3RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352155T>G , CM000685.2:g.1352155T>G GRCh38
NC_000023.10:g.1471048T>G , CM000685.1:g.1471048T>G GRCh37
NC_000023.9:g.1431048T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.354T>G MANE Select ENSP00000327890.4:p.Asp118Glu
ENST00000331035.9:c.354T>G ENSP00000327890.4:p.Asp118Glu
ENST00000381469.7:c.120T>G ENSP00000370878.2:p.Asp40Glu
ENST00000432757.6:c.120T>G ENSP00000414867.1:p.Asp40Glu
XM_005274431.3:c.354T>G XP_005274488.1:p.Asp118Glu
XM_005274432.1:c.354T>G XP_005274489.1:p.Asp118Glu
XR_247285.3:n.870+155A>C
XR_430488.2:n.1194+155A>C
XR_430490.2:n.869+155A>C
XR_951269.1:n.1398+155A>C
XR_951270.1:n.1415+155A>C
XR_951271.1:n.1466+155A>C
XR_951272.1:n.1402+155A>C
XR_951273.1:n.1329+155A>C
XR_951274.1:n.1333+155A>C
XR_951276.1:n.1346+155A>C
XR_951277.1:n.1398+155A>C
XR_951278.1:n.1398+155A>C
XR_951279.1:n.1398+155A>C
XR_951280.1:n.1398+155A>C
XR_951281.1:n.1398+155A>C
XR_951282.1:n.1243+155A>C
XR_951283.1:n.872+155A>C
XM_005274431.5:c.354T>G XP_005274488.1:p.Asp118Glu
XM_017029491.2:c.354T>G XP_016884980.1:p.Asp118Glu
XR_001755748.1:n.1189+155A>C
XR_001755751.1:n.1189+155A>C
XR_001755752.1:n.1189+155A>C
XR_001755754.1:n.1189+155A>C