Canonical Allele Identifier: CA2695227788
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.853329_853343del , CM000681.2:g.853329_853343del GRCh38
NC_000019.9:g.853329_853343del , CM000681.1:g.853329_853343del GRCh37
NC_000019.8:g.804329_804343del NCBI36
NG_009627.1:g.6039_6053del , LRG_57:g.6039_6053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.292_306del MANE Select ENSP00000263621.1:p.Val98_Gln102del
ENST00000263621.1:c.292_306del ENSP00000263621.1:p.Val98_Gln102del
ENST00000590230.5:c.292_306del ENSP00000466090.1:p.Val98_Gln102del
NM_001972.2:c.292_306del , LRG_57t1:c.292_306del NP_001963.1:p.Val98_Gln102del
XM_011527775.1:c.292_306del XP_011526077.1:p.Val98_Gln102del
XM_011527776.1:c.292_306del XP_011526078.1:p.Val98_Gln102del
NM_001972.3:c.292_306del NP_001963.1:p.Val98_Gln102del
NM_001972.4:c.292_306del MANE Select NP_001963.1:p.Val98_Gln102del