Canonical Allele Identifier: CA9026162

Gene: ELANE

Linked Data

• ClinVar Variation Id: 668758
• ClinVar RCV Id: RCV000827714 ; RCV001796260 ; RCV002264025
• dbSNP Id: rs143579306
• ExAC: 19:856138 C / A
• gnomAD v2: 19-856138-C-A
• gnomAD v3: 19-856138-C-A
• gnomAD v4: 19-856138-C-A
• MyVariant Identifiers: chr19:g.856138C>A (hg19) ; chr19:g.856138C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.856138C>A , CM000681.2:g.856138C>A	GRCh38
NC_000019.9:g.856138C>A , CM000681.1:g.856138C>A	GRCh37
NC_000019.8:g.807138C>A	NCBI36
NG_007274.1:g.1474C>A , LRG_46:g.1474C>A
NG_009627.1:g.8848C>A , LRG_57:g.8848C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263621.2:c.778C>A MANE Select	ENSP00000263621.1:p.Pro260Thr
ENST00000263621.1:c.778C>A	ENSP00000263621.1:p.Pro260Thr
ENST00000590230.5:c.778C>A	ENSP00000466090.1:p.Pro260Thr
NM_001972.2:c.778C>A , LRG_57t1:c.778C>A	NP_001963.1:p.Pro260Thr
XM_011527775.1:c.778C>A	XP_011526077.1:p.Pro260Thr
XM_011527776.1:c.778C>A	XP_011526078.1:p.Pro260Thr
NM_001972.3:c.778C>A	NP_001963.1:p.Pro260Thr
NM_001972.4:c.778C>A MANE Select	NP_001963.1:p.Pro260Thr