Canonical Allele Identifier: CA515393109

Gene: IL3RA

Linked Data

• COSMIC: COSM404112
• MyVariant Identifiers: chrX:g.1471245C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352352C>T , CM000685.2:g.1352352C>T	GRCh38
NC_000023.10:g.1471245C>T , CM000685.1:g.1471245C>T	GRCh37
NC_000023.9:g.1431245C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.462C>T MANE Select	ENSP00000327890.4:p.Tyr154=
ENST00000331035.9:c.462C>T	ENSP00000327890.4:p.Tyr154=
ENST00000381469.7:c.228C>T	ENSP00000370878.2:p.Tyr76=
ENST00000432757.6:c.228C>T	ENSP00000414867.1:p.Tyr76=
XM_005274431.3:c.462C>T	XP_005274488.1:p.Tyr154=
XM_005274432.1:c.459C>T	XP_005274489.1:p.Tyr153=
XR_247285.3:n.828G>A
XR_430488.2:n.1152G>A
XR_430490.2:n.827G>A
XR_951269.1:n.1356G>A
XR_951270.1:n.1373G>A
XR_951271.1:n.1424G>A
XR_951272.1:n.1360G>A
XR_951273.1:n.1287G>A
XR_951274.1:n.1291G>A
XR_951276.1:n.1304G>A
XR_951277.1:n.1356G>A
XR_951278.1:n.1356G>A
XR_951279.1:n.1356G>A
XR_951280.1:n.1356G>A
XR_951281.1:n.1356G>A
XR_951282.1:n.1201G>A
XR_951283.1:n.830G>A
XM_005274431.5:c.462C>T	XP_005274488.1:p.Tyr154=
XM_017029491.2:c.459C>T	XP_016884980.1:p.Tyr153=
XR_001755748.1:n.1147G>A
XR_001755751.1:n.1147G>A
XR_001755752.1:n.1147G>A
XR_001755754.1:n.1147G>A