Canonical Allele Identifier: CA9026107

Gene: ELANE

Linked Data

• dbSNP Id: rs775398593
• ExAC: 19:855820 T / C
• gnomAD v2: 19-855820-T-C
• gnomAD v4: 19-855820-T-C
• MyVariant Identifiers: chr19:g.855820T>C (hg19) ; chr19:g.855820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.855820T>C , CM000681.2:g.855820T>C	GRCh38
NC_000019.9:g.855820T>C , CM000681.1:g.855820T>C	GRCh37
NC_000019.8:g.806820T>C	NCBI36
NG_007274.1:g.1156T>C , LRG_46:g.1156T>C
NG_009627.1:g.8530T>C , LRG_57:g.8530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263621.2:c.597+26T>C MANE Select	ENSP00000263621.1:n.597+26T>C
ENST00000263621.1:c.597+26T>C	ENSP00000263621.1:n.597+26T>C
ENST00000590230.5:c.597+26T>C	ENSP00000466090.1:n.597+26T>C
NM_001972.2:c.597+26T>C , LRG_57t1:c.597+26T>C	NP_001963.1:n.597+26T>C
XM_011527775.1:c.597+26T>C	XP_011526077.1:n.597+26T>C
XM_011527776.1:c.597+26T>C	XP_011526078.1:n.597+26T>C
NM_001972.3:c.597+26T>C	NP_001963.1:n.597+26T>C
NM_001972.4:c.597+26T>C MANE Select	NP_001963.1:n.597+26T>C