Canonical Allele Identifier: CA2664186400

Gene: IL5RA

Linked Data

• gnomAD v4: 3-3076770-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3076770C>T , CM000665.2:g.3076770C>T	GRCh38
NC_000003.11:g.3118454C>T , CM000665.1:g.3118454C>T	GRCh37
NC_000003.10:g.3093454C>T	NCBI36
NG_029547.1:g.38605G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446632.7:c.995-143G>A MANE Select	ENSP00000412209.2:n.995-143G>A
ENST00000256452.7:c.995-143G>A	ENSP00000256452.3:n.995-143G>A
ENST00000418488.6:c.710-143G>A	ENSP00000388858.2:n.710-143G>A
ENST00000438560.5:c.995-143G>A	ENSP00000390753.1:n.995-143G>A
ENST00000446632.6:c.995-143G>A	ENSP00000412209.2:n.995-143G>A
NM_000564.4:c.995-143G>A	NP_000555.2:n.995-143G>A
NM_001243099.1:c.995-143G>A	NP_001230028.1:n.995-143G>A
NM_175726.3:c.995-143G>A	NP_783853.1:n.995-143G>A
XM_011533677.1:c.995-143G>A	XP_011531979.1:n.995-143G>A
XM_011533678.1:c.995-143G>A	XP_011531980.1:n.995-143G>A
XM_011533677.2:c.995-143G>A	XP_011531979.1:n.995-143G>A
XM_011533678.2:c.995-143G>A	XP_011531980.1:n.995-143G>A
NM_000564.5:c.995-143G>A	NP_000555.2:n.995-143G>A
NM_001243099.2:c.995-143G>A	NP_001230028.1:n.995-143G>A
NM_175726.4:c.995-143G>A MANE Select	NP_783853.1:n.995-143G>A