Canonical Allele Identifier: CA402914501

Gene: ELANE

Linked Data

• ClinVar Variation Id: 2947200
• ClinVar RCV Id: RCV003801390
• MyVariant Identifiers: chr19:g.852937C>G (hg19) ; chr19:g.852937C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.852937C>G , CM000681.2:g.852937C>G	GRCh38
NC_000019.9:g.852937C>G , CM000681.1:g.852937C>G	GRCh37
NC_000019.8:g.803937C>G	NCBI36
NG_009627.1:g.5647C>G , LRG_57:g.5647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263621.2:c.129C>G MANE Select	ENSP00000263621.1:p.Phe43Leu
ENST00000263621.1:c.129C>G	ENSP00000263621.1:p.Phe43Leu
ENST00000590230.5:c.129C>G	ENSP00000466090.1:p.Phe43Leu
NM_001972.2:c.129C>G , LRG_57t1:c.129C>G	NP_001963.1:p.Phe43Leu
XM_011527775.1:c.129C>G	XP_011526077.1:p.Phe43Leu
XM_011527776.1:c.129C>G	XP_011526078.1:p.Phe43Leu
NM_001972.3:c.129C>G	NP_001963.1:p.Phe43Leu
NM_001972.4:c.129C>G MANE Select	NP_001963.1:p.Phe43Leu