Canonical Allele Identifier: CA2692966366

Gene: IL3RA

Linked Data

• gnomAD v4: X-1352657-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352658del , CM000685.2:g.1352658del	GRCh38
NC_000023.10:g.1471551del , CM000685.1:g.1471551del	GRCh37
NC_000023.9:g.1431551del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.616+152del MANE Select	ENSP00000327890.4:n.616+152del
ENST00000331035.9:c.616+152del	ENSP00000327890.4:n.616+152del
ENST00000381469.7:c.382+152del	ENSP00000370878.2:n.382+152del
ENST00000432757.6:c.382+152del	ENSP00000414867.1:n.382+152del
XM_005274431.3:c.616+152del	XP_005274488.1:n.616+152del
XM_005274432.1:c.613+152del	XP_005274489.1:n.613+152del
XR_247285.3:n.670del
XR_430488.2:n.994del
XR_430490.2:n.669del
XR_951269.1:n.1198del
XR_951270.1:n.1215del
XR_951271.1:n.1198del
XR_951272.1:n.1202del
XR_951273.1:n.1129del
XR_951274.1:n.1133del
XR_951276.1:n.1146del
XR_951277.1:n.1198del
XR_951278.1:n.1198del
XR_951279.1:n.1198del
XR_951280.1:n.1198del
XR_951281.1:n.1198del
XR_951282.1:n.1043del
XR_951283.1:n.672del
XM_005274431.5:c.616+152del	XP_005274488.1:n.616+152del
XM_017029491.2:c.613+152del	XP_016884980.1:n.613+152del
XR_001755748.1:n.989del
XR_001755749.1:n.1006del
XR_001755750.1:n.989del
XR_001755751.1:n.989del
XR_001755752.1:n.989del
XR_001755753.1:n.993del
XR_001755754.1:n.989del
XR_001755755.1:n.920del
XR_001755756.1:n.671del
XR_001755757.1:n.924del
XR_001755758.1:n.937del
XR_001755759.1:n.785del
XR_001755760.2:n.723del
XR_001755761.1:n.673del
XR_001755762.1:n.669del