Canonical Allele Identifier: CA402914619
Gene: ELANE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.852960G>C , CM000681.2:g.852960G>C GRCh38
NC_000019.9:g.852960G>C , CM000681.1:g.852960G>C GRCh37
NC_000019.8:g.803960G>C NCBI36
NG_009627.1:g.5670G>C , LRG_57:g.5670G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.152G>C MANE Select ENSP00000263621.1:p.Gly51Ala
ENST00000263621.1:c.152G>C ENSP00000263621.1:p.Gly51Ala
ENST00000590230.5:c.152G>C ENSP00000466090.1:p.Gly51Ala
NM_001972.2:c.152G>C , LRG_57t1:c.152G>C NP_001963.1:p.Gly51Ala
XM_011527775.1:c.152G>C XP_011526077.1:p.Gly51Ala
XM_011527776.1:c.152G>C XP_011526078.1:p.Gly51Ala
NM_001972.3:c.152G>C NP_001963.1:p.Gly51Ala
NM_001972.4:c.152G>C MANE Select NP_001963.1:p.Gly51Ala