Canonical Allele Identifier: CA2317361388
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855640G= , CM000681.2:g.855640G= GRCh38
NC_000019.9:g.855640G= , CM000681.1:g.855640G= GRCh37
NC_000019.8:g.806640G= NCBI36
NG_007274.1:g.976G= , LRG_46:g.976G=
NG_009627.1:g.8350G= , LRG_57:g.8350G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.443G= MANE Select ENSP00000263621.1:p.Gly148=
ENST00000263621.1:c.443G= ENSP00000263621.1:p.Gly148=
ENST00000590230.5:c.443G= ENSP00000466090.1:p.Gly148=
NM_001972.2:c.443G= , LRG_57t1:c.443G= NP_001963.1:p.Gly148=
XM_011527775.1:c.443G= XP_011526077.1:p.Gly148=
XM_011527776.1:c.443G= XP_011526078.1:p.Gly148=
NM_001972.3:c.443G= NP_001963.1:p.Gly148=
NM_001972.4:c.443G= MANE Select NP_001963.1:p.Gly148=