Canonical Allele Identifier: CA2695227805
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855786_855793dup , CM000681.2:g.855786_855793dup GRCh38
NC_000019.9:g.855786_855793dup , CM000681.1:g.855786_855793dup GRCh37
NC_000019.8:g.806786_806793dup NCBI36
NG_007274.1:g.1122_1129dup , LRG_46:g.1122_1129dup
NG_009627.1:g.8496_8503dup , LRG_57:g.8496_8503dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.589_596dup MANE Select ENSP00000263621.1:p.Phe199LeufsTer16
ENST00000263621.1:c.589_596dup ENSP00000263621.1:p.Phe199LeufsTer16
ENST00000590230.5:c.589_596dup ENSP00000466090.1:p.Phe199LeufsTer16
NM_001972.2:c.589_596dup , LRG_57t1:c.589_596dup NP_001963.1:p.Phe199LeufsTer16
XM_011527775.1:c.589_596dup XP_011526077.1:p.Phe199LeufsTer16
XM_011527776.1:c.589_596dup XP_011526078.1:p.Phe199LeufsTer16
NM_001972.3:c.589_596dup NP_001963.1:p.Phe199LeufsTer16
NM_001972.4:c.589_596dup MANE Select NP_001963.1:p.Phe199LeufsTer16