Canonical Allele Identifier: CA402919543
Gene: ELANE HGNC NCBI

Linked Data

gnomAD v4: 19-856150-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856150A>T , CM000681.2:g.856150A>T GRCh38
NC_000019.9:g.856150A>T , CM000681.1:g.856150A>T GRCh37
NC_000019.8:g.807150A>T NCBI36
NG_007274.1:g.1486A>T , LRG_46:g.1486A>T
NG_009627.1:g.8860A>T , LRG_57:g.8860A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.790A>T MANE Select ENSP00000263621.1:p.Ser264Cys
ENST00000263621.1:c.790A>T ENSP00000263621.1:p.Ser264Cys
ENST00000590230.5:c.790A>T ENSP00000466090.1:p.Ser264Cys
NM_001972.2:c.790A>T , LRG_57t1:c.790A>T NP_001963.1:p.Ser264Cys
XM_011527775.1:c.790A>T XP_011526077.1:p.Ser264Cys
XM_011527776.1:c.790A>T XP_011526078.1:p.Ser264Cys
NM_001972.3:c.790A>T NP_001963.1:p.Ser264Cys
NM_001972.4:c.790A>T MANE Select NP_001963.1:p.Ser264Cys