Canonical Allele Identifier: CA2580096965
Gene: ELANE HGNC NCBI

Linked Data

ClinVar Variation Id: 2004561
ClinVar RCV Id: RCV002816182

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855778_855794dup , CM000681.2:g.855778_855794dup GRCh38
NC_000019.9:g.855778_855794dup , CM000681.1:g.855778_855794dup GRCh37
NC_000019.8:g.806778_806794dup NCBI36
NG_007274.1:g.1114_1130dup , LRG_46:g.1114_1130dup
NG_009627.1:g.8488_8504dup , LRG_57:g.8488_8504dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.581_597dup MANE Select ENSP00000263621.1:p.Gly200ArgfsTer18
ENST00000263621.1:c.581_597dup ENSP00000263621.1:p.Gly200ArgfsTer18
ENST00000590230.5:c.581_597dup ENSP00000466090.1:p.Gly200ArgfsTer18
NM_001972.2:c.581_597dup , LRG_57t1:c.581_597dup NP_001963.1:p.Gly200ArgfsTer18
XM_011527775.1:c.581_597dup XP_011526077.1:p.Gly200ArgfsTer18
XM_011527776.1:c.581_597dup XP_011526078.1:p.Gly200ArgfsTer18
NM_001972.3:c.581_597dup NP_001963.1:p.Gly200ArgfsTer18
NM_001972.4:c.581_597dup MANE Select NP_001963.1:p.Gly200ArgfsTer18