Canonical Allele Identifier: CA412245879

Gene: IL3RA

Linked Data

• MyVariant Identifiers: chrX:g.1471232A>C (hg19) ; chrX:g.1352339A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352339A>C , CM000685.2:g.1352339A>C	GRCh38
NC_000023.10:g.1471232A>C , CM000685.1:g.1471232A>C	GRCh37
NC_000023.9:g.1431232A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.449A>C MANE Select	ENSP00000327890.4:p.Glu150Ala
ENST00000331035.9:c.449A>C	ENSP00000327890.4:p.Glu150Ala
ENST00000381469.7:c.215A>C	ENSP00000370878.2:p.Glu72Ala
ENST00000432757.6:c.215A>C	ENSP00000414867.1:p.Glu72Ala
XM_005274431.3:c.449A>C	XP_005274488.1:p.Glu150Ala
XM_005274432.1:c.446A>C	XP_005274489.1:p.Glu149Ala
XR_247285.3:n.841T>G
XR_430488.2:n.1165T>G
XR_430490.2:n.840T>G
XR_951269.1:n.1369T>G
XR_951270.1:n.1386T>G
XR_951271.1:n.1437T>G
XR_951272.1:n.1373T>G
XR_951273.1:n.1300T>G
XR_951274.1:n.1304T>G
XR_951276.1:n.1317T>G
XR_951277.1:n.1369T>G
XR_951278.1:n.1369T>G
XR_951279.1:n.1369T>G
XR_951280.1:n.1369T>G
XR_951281.1:n.1369T>G
XR_951282.1:n.1214T>G
XR_951283.1:n.843T>G
XM_005274431.5:c.449A>C	XP_005274488.1:p.Glu150Ala
XM_017029491.2:c.446A>C	XP_016884980.1:p.Glu149Ala
XR_001755748.1:n.1160T>G
XR_001755751.1:n.1160T>G
XR_001755752.1:n.1160T>G
XR_001755754.1:n.1160T>G