Canonical Allele Identifier: CA402918971

Gene: ELANE

Linked Data

• ClinVar Variation Id: 855162
• ClinVar RCV Id: RCV001796360
• dbSNP Id: rs2035674370
• MyVariant Identifiers: chr19:g.855994A>G (hg19) ; chr19:g.855994A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.855994A>G , CM000681.2:g.855994A>G	GRCh38
NC_000019.9:g.855994A>G , CM000681.1:g.855994A>G	GRCh37
NC_000019.8:g.806994A>G	NCBI36
NG_007274.1:g.1330A>G , LRG_46:g.1330A>G
NG_009627.1:g.8704A>G , LRG_57:g.8704A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263621.2:c.634A>G MANE Select	ENSP00000263621.1:p.Ile212Val
ENST00000263621.1:c.634A>G	ENSP00000263621.1:p.Ile212Val
ENST00000590230.5:c.634A>G	ENSP00000466090.1:p.Ile212Val
NM_001972.2:c.634A>G , LRG_57t1:c.634A>G	NP_001963.1:p.Ile212Val
XM_011527775.1:c.634A>G	XP_011526077.1:p.Ile212Val
XM_011527776.1:c.634A>G	XP_011526078.1:p.Ile212Val
NM_001972.3:c.634A>G	NP_001963.1:p.Ile212Val
NM_001972.4:c.634A>G MANE Select	NP_001963.1:p.Ile212Val