Canonical Allele Identifier: CA402917975
Gene: ELANE HGNC NCBI

Linked Data

dbSNP Id: rs2035665078

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855619A>G , CM000681.2:g.855619A>G GRCh38
NC_000019.9:g.855619A>G , CM000681.1:g.855619A>G GRCh37
NC_000019.8:g.806619A>G NCBI36
NG_007274.1:g.955A>G , LRG_46:g.955A>G
NG_009627.1:g.8329A>G , LRG_57:g.8329A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.422A>G MANE Select ENSP00000263621.1:p.Gln141Arg
ENST00000263621.1:c.422A>G ENSP00000263621.1:p.Gln141Arg
ENST00000590230.5:c.422A>G ENSP00000466090.1:p.Gln141Arg
NM_001972.2:c.422A>G , LRG_57t1:c.422A>G NP_001963.1:p.Gln141Arg
XM_011527775.1:c.422A>G XP_011526077.1:p.Gln141Arg
XM_011527776.1:c.422A>G XP_011526078.1:p.Gln141Arg
NM_001972.3:c.422A>G NP_001963.1:p.Gln141Arg
NM_001972.4:c.422A>G MANE Select NP_001963.1:p.Gln141Arg