Canonical Allele Identifier: CA504684967
Gene: ELANE HGNC NCBI

Linked Data

COSMIC: COSM310850
MyVariant Identifiers: chr19:g.853337C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.853337C>A , CM000681.2:g.853337C>A GRCh38
NC_000019.9:g.853337C>A , CM000681.1:g.853337C>A GRCh37
NC_000019.8:g.804337C>A NCBI36
NG_009627.1:g.6047C>A , LRG_57:g.6047C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.300C>A MANE Select ENSP00000263621.1:p.Ala100=
ENST00000263621.1:c.300C>A ENSP00000263621.1:p.Ala100=
ENST00000590230.5:c.300C>A ENSP00000466090.1:p.Ala100=
NM_001972.2:c.300C>A , LRG_57t1:c.300C>A NP_001963.1:p.Ala100=
XM_011527775.1:c.300C>A XP_011526077.1:p.Ala100=
XM_011527776.1:c.300C>A XP_011526078.1:p.Ala100=
NM_001972.3:c.300C>A NP_001963.1:p.Ala100=
NM_001972.4:c.300C>A MANE Select NP_001963.1:p.Ala100=