Canonical Allele Identifier: CA906128818

Gene: IL5RA

Linked Data

• dbSNP Id: rs1296652800
• gnomAD v3: 3-3076831-TAG-T
• gnomAD v4: 3-3076831-TAG-T
• MyVariant Identifiers: chr3:g.3118516_3118517del (hg19) ; chr3:g.3076832_3076833del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3076832_3076833del , CM000665.2:g.3076832_3076833del	GRCh38
NC_000003.11:g.3118516_3118517del , CM000665.1:g.3118516_3118517del	GRCh37
NC_000003.10:g.3093516_3093517del	NCBI36
NG_029547.1:g.38542_38543del

Transcript Alleles

HGVS	Amino-acid change
ENST00000446632.7:c.995-206_995-205del MANE Select	ENSP00000412209.2:n.995-206_995-205del
ENST00000256452.7:c.995-206_995-205del	ENSP00000256452.3:n.995-206_995-205del
ENST00000418488.6:c.710-206_710-205del	ENSP00000388858.2:n.710-206_710-205del
ENST00000438560.5:c.995-206_995-205del	ENSP00000390753.1:n.995-206_995-205del
ENST00000446632.6:c.995-206_995-205del	ENSP00000412209.2:n.995-206_995-205del
NM_000564.4:c.995-206_995-205del	NP_000555.2:n.995-206_995-205del
NM_001243099.1:c.995-206_995-205del	NP_001230028.1:n.995-206_995-205del
NM_175726.3:c.995-206_995-205del	NP_783853.1:n.995-206_995-205del
XM_011533677.1:c.995-206_995-205del	XP_011531979.1:n.995-206_995-205del
XM_011533678.1:c.995-206_995-205del	XP_011531980.1:n.995-206_995-205del
XM_011533677.2:c.995-206_995-205del	XP_011531979.1:n.995-206_995-205del
XM_011533678.2:c.995-206_995-205del	XP_011531980.1:n.995-206_995-205del
NM_000564.5:c.995-206_995-205del	NP_000555.2:n.995-206_995-205del
NM_001243099.2:c.995-206_995-205del	NP_001230028.1:n.995-206_995-205del
NM_175726.4:c.995-206_995-205del MANE Select	NP_783853.1:n.995-206_995-205del