Canonical Allele Identifier: CA504686444

Gene: ELANE

Linked Data

• ClinVar Variation Id: 725648
• ClinVar RCV Id: RCV000899740
• dbSNP Id: rs1599294640
• MyVariant Identifiers: chr19:g.855990G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.855990G>A , CM000681.2:g.855990G>A	GRCh38
NC_000019.9:g.855990G>A , CM000681.1:g.855990G>A	GRCh37
NC_000019.8:g.806990G>A	NCBI36
NG_007274.1:g.1326G>A , LRG_46:g.1326G>A
NG_009627.1:g.8700G>A , LRG_57:g.8700G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263621.2:c.630G>A MANE Select	ENSP00000263621.1:p.Gly210=
ENST00000263621.1:c.630G>A	ENSP00000263621.1:p.Gly210=
ENST00000590230.5:c.630G>A	ENSP00000466090.1:p.Gly210=
NM_001972.2:c.630G>A , LRG_57t1:c.630G>A	NP_001963.1:p.Gly210=
XM_011527775.1:c.630G>A	XP_011526077.1:p.Gly210=
XM_011527776.1:c.630G>A	XP_011526078.1:p.Gly210=
NM_001972.3:c.630G>A	NP_001963.1:p.Gly210=
NM_001972.4:c.630G>A MANE Select	NP_001963.1:p.Gly210=