Canonical Allele Identifier: CA412245980

Gene: IL3RA

Linked Data

• MyVariant Identifiers: chrX:g.1471250C>A (hg19) ; chrX:g.1352357C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352357C>A , CM000685.2:g.1352357C>A	GRCh38
NC_000023.10:g.1471250C>A , CM000685.1:g.1471250C>A	GRCh37
NC_000023.9:g.1431250C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.467C>A MANE Select	ENSP00000327890.4:p.Thr156Lys
ENST00000331035.9:c.467C>A	ENSP00000327890.4:p.Thr156Lys
ENST00000381469.7:c.233C>A	ENSP00000370878.2:p.Thr78Lys
ENST00000432757.6:c.233C>A	ENSP00000414867.1:p.Thr78Lys
XM_005274431.3:c.467C>A	XP_005274488.1:p.Thr156Lys
XM_005274432.1:c.464C>A	XP_005274489.1:p.Thr155Lys
XR_247285.3:n.823G>T
XR_430488.2:n.1147G>T
XR_430490.2:n.822G>T
XR_951269.1:n.1351G>T
XR_951270.1:n.1368G>T
XR_951271.1:n.1419G>T
XR_951272.1:n.1355G>T
XR_951273.1:n.1282G>T
XR_951274.1:n.1286G>T
XR_951276.1:n.1299G>T
XR_951277.1:n.1351G>T
XR_951278.1:n.1351G>T
XR_951279.1:n.1351G>T
XR_951280.1:n.1351G>T
XR_951281.1:n.1351G>T
XR_951282.1:n.1196G>T
XR_951283.1:n.825G>T
XM_005274431.5:c.467C>A	XP_005274488.1:p.Thr156Lys
XM_017029491.2:c.464C>A	XP_016884980.1:p.Thr155Lys
XR_001755748.1:n.1142G>T
XR_001755751.1:n.1142G>T
XR_001755752.1:n.1142G>T
XR_001755754.1:n.1142G>T