Canonical Allele Identifier: CA1341418335
Gene: IL5RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3087948T>A , CM000665.2:g.3087948T>A GRCh38
NC_000003.11:g.3129632T>A , CM000665.1:g.3129632T>A GRCh37
NC_000003.10:g.3104632T>A NCBI36
NG_029547.1:g.27427A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000446632.7:c.994+4276A>T MANE Select ENSP00000412209.2:n.994+4276A>T
ENST00000256452.7:c.994+4276A>T ENSP00000256452.3:n.994+4276A>T
ENST00000418488.6:c.709+9922A>T ENSP00000388858.2:n.709+9922A>T
ENST00000438560.5:c.994+4276A>T ENSP00000390753.1:n.994+4276A>T
ENST00000446632.6:c.994+4276A>T ENSP00000412209.2:n.994+4276A>T
NM_000564.4:c.994+4276A>T NP_000555.2:n.994+4276A>T
NM_001243099.1:c.994+4276A>T NP_001230028.1:n.994+4276A>T
NM_175726.3:c.994+4276A>T NP_783853.1:n.994+4276A>T
XM_011533677.1:c.994+4276A>T XP_011531979.1:n.994+4276A>T
XM_011533678.1:c.994+4276A>T XP_011531980.1:n.994+4276A>T
XM_011533677.2:c.994+4276A>T XP_011531979.1:n.994+4276A>T
XM_011533678.2:c.994+4276A>T XP_011531980.1:n.994+4276A>T
NM_000564.5:c.994+4276A>T NP_000555.2:n.994+4276A>T
NM_001243099.2:c.994+4276A>T NP_001230028.1:n.994+4276A>T
NM_175726.4:c.994+4276A>T MANE Select NP_783853.1:n.994+4276A>T