Canonical Allele Identifier: CA504881764
Gene: ELANE HGNC NCBI

Linked Data

dbSNP Id: rs1265303415
gnomAD v2: 19-855599-G-A
gnomAD v4: 19-855599-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855599G>A , CM000681.2:g.855599G>A GRCh38
NC_000019.9:g.855599G>A , CM000681.1:g.855599G>A GRCh37
NC_000019.8:g.806599G>A NCBI36
NG_007274.1:g.935G>A , LRG_46:g.935G>A
NG_009627.1:g.8309G>A , LRG_57:g.8309G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.402G>A MANE Select ENSP00000263621.1:p.Gln134=
ENST00000263621.1:c.402G>A ENSP00000263621.1:p.Gln134=
ENST00000590230.5:c.402G>A ENSP00000466090.1:p.Gln134=
NM_001972.2:c.402G>A , LRG_57t1:c.402G>A NP_001963.1:p.Gln134=
XM_011527775.1:c.402G>A XP_011526077.1:p.Gln134=
XM_011527776.1:c.402G>A XP_011526078.1:p.Gln134=
NM_001972.3:c.402G>A NP_001963.1:p.Gln134=
NM_001972.4:c.402G>A MANE Select NP_001963.1:p.Gln134=