Canonical Allele Identifier: CA402917959

Gene: ELANE

Linked Data

• gnomAD v4: 19-855616-C-A
• MyVariant Identifiers: chr19:g.855616C>A (hg19) ; chr19:g.855616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.855616C>A , CM000681.2:g.855616C>A	GRCh38
NC_000019.9:g.855616C>A , CM000681.1:g.855616C>A	GRCh37
NC_000019.8:g.806616C>A	NCBI36
NG_007274.1:g.952C>A , LRG_46:g.952C>A
NG_009627.1:g.8326C>A , LRG_57:g.8326C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263621.2:c.419C>A MANE Select	ENSP00000263621.1:p.Ala140Asp
ENST00000263621.1:c.419C>A	ENSP00000263621.1:p.Ala140Asp
ENST00000590230.5:c.419C>A	ENSP00000466090.1:p.Ala140Asp
NM_001972.2:c.419C>A , LRG_57t1:c.419C>A	NP_001963.1:p.Ala140Asp
XM_011527775.1:c.419C>A	XP_011526077.1:p.Ala140Asp
XM_011527776.1:c.419C>A	XP_011526078.1:p.Ala140Asp
NM_001972.3:c.419C>A	NP_001963.1:p.Ala140Asp
NM_001972.4:c.419C>A MANE Select	NP_001963.1:p.Ala140Asp