Canonical Allele Identifier: CA10331591
Community Standard Title: NM_002183.4(IL3RA):c.257C>T (p.Ala86Val)
Gene: IL3RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1348504C>T , CM000685.2:g.1348504C>T GRCh38
NC_000023.10:g.1467397C>T , CM000685.1:g.1467397C>T GRCh37
NC_000023.9:g.1427397C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.257C>T MANE Select ENSP00000327890.4:p.Ala86Val
ENST00000331035.9:c.257C>T ENSP00000327890.4:p.Ala86Val
ENST00000381469.7:c.65-3596C>T ENSP00000370878.2:n.65-3596C>T
ENST00000432757.6:c.65-3596C>T ENSP00000414867.1:n.65-3596C>T
XM_005274431.3:c.257C>T XP_005274488.1:p.Ala86Val
XM_005274431.5:c.257C>T XP_005274488.1:p.Ala86Val
XM_005274432.1:c.257C>T XP_005274489.1:p.Ala86Val
XM_017029491.2:c.257C>T XP_016884980.1:p.Ala86Val
XR_001755748.1:n.1189+3806G>A
XR_247285.3:n.870+3806G>A
XR_430488.2:n.1194+3806G>A
XR_430490.2:n.869+3806G>A
XR_951269.1:n.1398+3806G>A
XR_951270.1:n.1415+3806G>A
XR_951271.1:n.1466+3806G>A
XR_951272.1:n.1402+3806G>A
XR_951273.1:n.1329+3806G>A
XR_951274.1:n.1333+3806G>A
XR_951276.1:n.1346+3806G>A
XR_951277.1:n.1398+3806G>A
XR_951278.1:n.1398+3806G>A
XR_951282.1:n.1243+3806G>A
XR_951283.1:n.872+3806G>A