Canonical Allele Identifier: CA9026119
Gene: ELANE HGNC NCBI

Linked Data

dbSNP Id: rs751761755
gnomAD v2: 19-855958-G-T
gnomAD v4: 19-855958-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855958G>T , CM000681.2:g.855958G>T GRCh38
NC_000019.9:g.855958G>T , CM000681.1:g.855958G>T GRCh37
NC_000019.8:g.806958G>T NCBI36
NG_007274.1:g.1294G>T , LRG_46:g.1294G>T
NG_009627.1:g.8668G>T , LRG_57:g.8668G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.598G>T MANE Select ENSP00000263621.1:p.Gly200Trp
ENST00000263621.1:c.598G>T ENSP00000263621.1:p.Gly200Trp
ENST00000590230.5:c.598G>T ENSP00000466090.1:p.Gly200Trp
NM_001972.2:c.598G>T , LRG_57t1:c.598G>T NP_001963.1:p.Gly200Trp
XM_011527775.1:c.598G>T XP_011526077.1:p.Gly200Trp
XM_011527776.1:c.598G>T XP_011526078.1:p.Gly200Trp
NM_001972.3:c.598G>T NP_001963.1:p.Gly200Trp
NM_001972.4:c.598G>T MANE Select NP_001963.1:p.Gly200Trp