Canonical Allele Identifier: CA2317361639
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856029C= , CM000681.2:g.856029C= GRCh38
NC_000019.9:g.856029C= , CM000681.1:g.856029C= GRCh37
NC_000019.8:g.807029C= NCBI36
NG_007274.1:g.1365C= , LRG_46:g.1365C=
NG_009627.1:g.8739C= , LRG_57:g.8739C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.669C= MANE Select ENSP00000263621.1:p.Cys223=
ENST00000263621.1:c.669C= ENSP00000263621.1:p.Cys223=
ENST00000590230.5:c.669C= ENSP00000466090.1:p.Cys223=
NM_001972.2:c.669C= , LRG_57t1:c.669C= NP_001963.1:p.Cys223=
XM_011527775.1:c.669C= XP_011526077.1:p.Cys223=
XM_011527776.1:c.669C= XP_011526078.1:p.Cys223=
NM_001972.3:c.669C= NP_001963.1:p.Cys223=
NM_001972.4:c.669C= MANE Select NP_001963.1:p.Cys223=