Canonical Allele Identifier: CA2580096958
Gene: ELANE HGNC NCBI

Linked Data

ClinVar Variation Id: 2029666
ClinVar RCV Id: RCV002880934

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.853252_853269dup , CM000681.2:g.853252_853269dup GRCh38
NC_000019.9:g.853252_853269dup , CM000681.1:g.853252_853269dup GRCh37
NC_000019.8:g.804252_804269dup NCBI36
NG_009627.1:g.5962_5979dup , LRG_57:g.5962_5979dup

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.225-10_232dup
ENST00000263621.1:c.225-10_232dup
ENST00000590230.5:c.225-10_232dup
NM_001972.2:c.225-10_232dup , LRG_57t1:c.225-10_232dup
XM_011527775.1:c.225-10_232dup
XM_011527776.1:c.225-10_232dup
NM_001972.3:c.225-10_232dup
NM_001972.4:c.225-10_232dup