Canonical Allele Identifier: CA2695227802
Gene: ELANE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855781_855785dup , CM000681.2:g.855781_855785dup GRCh38
NC_000019.9:g.855781_855785dup , CM000681.1:g.855781_855785dup GRCh37
NC_000019.8:g.806781_806785dup NCBI36
NG_007274.1:g.1117_1121dup , LRG_46:g.1117_1121dup
NG_009627.1:g.8491_8495dup , LRG_57:g.8491_8495dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.584_588dup MANE Select ENSP00000263621.1:p.Val197ProfsTer17
ENST00000263621.1:c.584_588dup ENSP00000263621.1:p.Val197ProfsTer17
ENST00000590230.5:c.584_588dup ENSP00000466090.1:p.Val197ProfsTer17
NM_001972.2:c.584_588dup , LRG_57t1:c.584_588dup NP_001963.1:p.Val197ProfsTer17
XM_011527775.1:c.584_588dup XP_011526077.1:p.Val197ProfsTer17
XM_011527776.1:c.584_588dup XP_011526078.1:p.Val197ProfsTer17
NM_001972.3:c.584_588dup NP_001963.1:p.Val197ProfsTer17
NM_001972.4:c.584_588dup MANE Select NP_001963.1:p.Val197ProfsTer17