Canonical Allele Identifier: CA515392948

Gene: IL3RA

Linked Data

• MyVariant Identifiers: chrX:g.1471081G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352188G>T , CM000685.2:g.1352188G>T	GRCh38
NC_000023.10:g.1471081G>T , CM000685.1:g.1471081G>T	GRCh37
NC_000023.9:g.1431081G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.387G>T MANE Select	ENSP00000327890.4:p.Gly129=
ENST00000331035.9:c.387G>T	ENSP00000327890.4:p.Gly129=
ENST00000381469.7:c.153G>T	ENSP00000370878.2:p.Gly51=
ENST00000432757.6:c.153G>T	ENSP00000414867.1:p.Gly51=
XM_005274431.3:c.387G>T	XP_005274488.1:p.Gly129=
XM_005274432.1:c.387G>T	XP_005274489.1:p.Gly129=
XR_247285.3:n.870+122C>A
XR_430488.2:n.1194+122C>A
XR_430490.2:n.869+122C>A
XR_951269.1:n.1398+122C>A
XR_951270.1:n.1415+122C>A
XR_951271.1:n.1466+122C>A
XR_951272.1:n.1402+122C>A
XR_951273.1:n.1329+122C>A
XR_951274.1:n.1333+122C>A
XR_951276.1:n.1346+122C>A
XR_951277.1:n.1398+122C>A
XR_951278.1:n.1398+122C>A
XR_951279.1:n.1398+122C>A
XR_951280.1:n.1398+122C>A
XR_951281.1:n.1398+122C>A
XR_951282.1:n.1243+122C>A
XR_951283.1:n.872+122C>A
XM_005274431.5:c.387G>T	XP_005274488.1:p.Gly129=
XM_017029491.2:c.387G>T	XP_016884980.1:p.Gly129=
XR_001755748.1:n.1189+122C>A
XR_001755751.1:n.1189+122C>A
XR_001755752.1:n.1189+122C>A
XR_001755754.1:n.1189+122C>A