Canonical Allele Identifier: CA412245909

Gene: IL3RA

Linked Data

• MyVariant Identifiers: chrX:g.1471237C>A (hg19) ; chrX:g.1352344C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352344C>A , CM000685.2:g.1352344C>A	GRCh38
NC_000023.10:g.1471237C>A , CM000685.1:g.1471237C>A	GRCh37
NC_000023.9:g.1431237C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.454C>A MANE Select	ENSP00000327890.4:p.Leu152Ile
ENST00000331035.9:c.454C>A	ENSP00000327890.4:p.Leu152Ile
ENST00000381469.7:c.220C>A	ENSP00000370878.2:p.Leu74Ile
ENST00000432757.6:c.220C>A	ENSP00000414867.1:p.Leu74Ile
XM_005274431.3:c.454C>A	XP_005274488.1:p.Leu152Ile
XM_005274432.1:c.451C>A	XP_005274489.1:p.Leu151Ile
XR_247285.3:n.836G>T
XR_430488.2:n.1160G>T
XR_430490.2:n.835G>T
XR_951269.1:n.1364G>T
XR_951270.1:n.1381G>T
XR_951271.1:n.1432G>T
XR_951272.1:n.1368G>T
XR_951273.1:n.1295G>T
XR_951274.1:n.1299G>T
XR_951276.1:n.1312G>T
XR_951277.1:n.1364G>T
XR_951278.1:n.1364G>T
XR_951279.1:n.1364G>T
XR_951280.1:n.1364G>T
XR_951281.1:n.1364G>T
XR_951282.1:n.1209G>T
XR_951283.1:n.838G>T
XM_005274431.5:c.454C>A	XP_005274488.1:p.Leu152Ile
XM_017029491.2:c.451C>A	XP_016884980.1:p.Leu151Ile
XR_001755748.1:n.1155G>T
XR_001755751.1:n.1155G>T
XR_001755752.1:n.1155G>T
XR_001755754.1:n.1155G>T