Canonical Allele Identifier: CA2830536159

Gene: EIF4A2 SNORA63B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186786420del , CM000665.2:g.186786420del	GRCh38
NC_000003.11:g.186504209del , CM000665.1:g.186504209del	GRCh37
NC_000003.10:g.187986903del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323963.10:c.628-82del (EIF4A2) MANE Select	ENSP00000326381.5:n.628-82del
ENST00000323963.9:c.628-82del (EIF4A2)	ENSP00000326381.5:n.628-82del
ENST00000425053.5:c.628-82del (EIF4A2)	ENSP00000413529.1:n.628-82del
ENST00000426808.5:c.*197-82del (EIF4A2)	ENSP00000392686.1:n.*197-82del
ENST00000429589.5:c.*197-82del (EIF4A2)	ENSP00000388237.1:n.*197-82del
ENST00000440191.6:c.631-82del (EIF4A2)	ENSP00000398370.2:n.631-82del
ENST00000443963.5:c.*197-82del (EIF4A2)	ENSP00000402313.1:n.*197-82del
ENST00000465792.1:n.345del (EIF4A2)
ENST00000466362.1:n.467del (EIF4A2)
ENST00000468362.5:n.201-82del (EIF4A2)
ENST00000475653.5:n.506-82del (EIF4A2)
ENST00000485101.5:n.1853del (EIF4A2)
ENST00000492144.5:n.168-82del (EIF4A2)
NM_001967.3:c.628-82del (EIF4A2)	NP_001958.2:n.628-82del
NR_145766.1:n.98del (SNORA63B)
NM_001967.4:c.628-82del (EIF4A2) MANE Select	NP_001958.2:n.628-82del