Canonical Allele Identifier: CA9026163
Gene: ELANE HGNC NCBI

Linked Data

ClinVar Variation Id: 2926000
ClinVar RCV Id: RCV003786286
dbSNP Id: rs373765150
gnomAD v2: 19-856139-C-T
gnomAD v4: 19-856139-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856139C>T , CM000681.2:g.856139C>T GRCh38
NC_000019.9:g.856139C>T , CM000681.1:g.856139C>T GRCh37
NC_000019.8:g.807139C>T NCBI36
NG_007274.1:g.1475C>T , LRG_46:g.1475C>T
NG_009627.1:g.8849C>T , LRG_57:g.8849C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.779C>T MANE Select ENSP00000263621.1:p.Pro260Leu
ENST00000263621.1:c.779C>T ENSP00000263621.1:p.Pro260Leu
ENST00000590230.5:c.779C>T ENSP00000466090.1:p.Pro260Leu
NM_001972.2:c.779C>T , LRG_57t1:c.779C>T NP_001963.1:p.Pro260Leu
XM_011527775.1:c.779C>T XP_011526077.1:p.Pro260Leu
XM_011527776.1:c.779C>T XP_011526078.1:p.Pro260Leu
NM_001972.3:c.779C>T NP_001963.1:p.Pro260Leu
NM_001972.4:c.779C>T MANE Select NP_001963.1:p.Pro260Leu