Canonical Allele Identifier: CA2411852751

Gene: IL3RA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352672G= , CM000685.2:g.1352672G=	GRCh38
NC_000023.10:g.1471565G= , CM000685.1:g.1471565G=	GRCh37
NC_000023.9:g.1431565G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331035.10:c.616+166G= MANE Select	ENSP00000327890.4:n.616+166G=
ENST00000331035.9:c.616+166G=	ENSP00000327890.4:n.616+166G=
ENST00000381469.7:c.382+166G=	ENSP00000370878.2:n.382+166G=
ENST00000432757.6:c.382+166G=	ENSP00000414867.1:n.382+166G=
XM_005274431.3:c.616+166G=	XP_005274488.1:n.616+166G=
XM_005274432.1:c.613+166G=	XP_005274489.1:n.613+166G=
XR_247285.3:n.656C=
XR_430488.2:n.980C=
XR_430490.2:n.655C=
XR_951269.1:n.1184C=
XR_951270.1:n.1201C=
XR_951271.1:n.1184C=
XR_951272.1:n.1188C=
XR_951273.1:n.1115C=
XR_951274.1:n.1119C=
XR_951276.1:n.1132C=
XR_951277.1:n.1184C=
XR_951278.1:n.1184C=
XR_951279.1:n.1184C=
XR_951280.1:n.1184C=
XR_951281.1:n.1184C=
XR_951282.1:n.1029C=
XR_951283.1:n.658C=
XM_005274431.5:c.616+166G=	XP_005274488.1:n.616+166G=
XM_017029491.2:c.613+166G=	XP_016884980.1:n.613+166G=
XR_001755748.1:n.975C=
XR_001755749.1:n.992C=
XR_001755750.1:n.975C=
XR_001755751.1:n.975C=
XR_001755752.1:n.975C=
XR_001755753.1:n.979C=
XR_001755754.1:n.975C=
XR_001755755.1:n.906C=
XR_001755756.1:n.657C=
XR_001755757.1:n.910C=
XR_001755758.1:n.923C=
XR_001755759.1:n.771C=
XR_001755760.2:n.709C=
XR_001755761.1:n.659C=
XR_001755762.1:n.655C=