Canonical Allele Identifier: CA2695227790
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.853332_853337dup , CM000681.2:g.853332_853337dup GRCh38
NC_000019.9:g.853332_853337dup , CM000681.1:g.853332_853337dup GRCh37
NC_000019.8:g.804332_804337dup NCBI36
NG_009627.1:g.6042_6047dup , LRG_57:g.6042_6047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.295_300dup MANE Select ENSP00000263621.1:p.Ala100_Val101insPheAla
ENST00000263621.1:c.295_300dup ENSP00000263621.1:p.Ala100_Val101insPheAla
ENST00000590230.5:c.295_300dup ENSP00000466090.1:p.Ala100_Val101insPheAla
NM_001972.2:c.295_300dup , LRG_57t1:c.295_300dup NP_001963.1:p.Ala100_Val101insPheAla
XM_011527775.1:c.295_300dup XP_011526077.1:p.Ala100_Val101insPheAla
XM_011527776.1:c.295_300dup XP_011526078.1:p.Ala100_Val101insPheAla
NM_001972.3:c.295_300dup NP_001963.1:p.Ala100_Val101insPheAla
NM_001972.4:c.295_300dup MANE Select NP_001963.1:p.Ala100_Val101insPheAla