Canonical Allele Identifier: CA2695227818
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856016del , CM000681.2:g.856016del GRCh38
NC_000019.9:g.856016del , CM000681.1:g.856016del GRCh37
NC_000019.8:g.807016del NCBI36
NG_007274.1:g.1352del , LRG_46:g.1352del
NG_009627.1:g.8726del , LRG_57:g.8726del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.656del MANE Select ENSP00000263621.1:p.Val219AlafsTer21
ENST00000263621.1:c.656del ENSP00000263621.1:p.Val219AlafsTer21
ENST00000590230.5:c.656del ENSP00000466090.1:p.Val219AlafsTer21
NM_001972.2:c.656del , LRG_57t1:c.656del NP_001963.1:p.Val219AlafsTer21
XM_011527775.1:c.656del XP_011526077.1:p.Val219AlafsTer21
XM_011527776.1:c.656del XP_011526078.1:p.Val219AlafsTer21
NM_001972.3:c.656del NP_001963.1:p.Val219AlafsTer21
NM_001972.4:c.656del MANE Select NP_001963.1:p.Val219AlafsTer21