Canonical Allele Identifier: CA2580079627
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1774392
ClinVar RCV Id: RCV002392394

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824384_127824396del , CM000671.2:g.127824384_127824396del GRCh38
NC_000009.11:g.130586663_130586675del , CM000671.1:g.130586663_130586675del GRCh37
NC_000009.10:g.129626484_129626496del NCBI36
NG_009551.1:g.35373_35385del , LRG_589:g.35373_35385del

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.496_508del ENSP00000479015.1:p.Asp166ArgfsTer7
ENST00000373203.9:c.1042_1054del MANE Select ENSP00000362299.4:p.Asp348ArgfsTer7
ENST00000344849.4:c.1042_1054del ENSP00000341917.3:p.Asp348ArgfsTer7
ENST00000373203.8:c.1042_1054del ENSP00000362299.4:p.Asp348ArgfsTer7
ENST00000480266.5:c.496_508del ENSP00000479015.1:p.Asp166ArgfsTer7
ENST00000486329.1:n.10_22del
NM_000118.3:c.1042_1054del , LRG_589t1:c.1042_1054del NP_000109.1:p.Asp348ArgfsTer7
NM_001114753.2:c.1042_1054del , LRG_589t2:c.1042_1054del NP_001108225.1:p.Asp348ArgfsTer7
NM_001278138.1:c.496_508del NP_001265067.1:p.Asp166ArgfsTer7
NM_001114753.3:c.1042_1054del MANE Select NP_001108225.1:p.Asp348ArgfsTer7
NM_001278138.2:c.496_508del NP_001265067.1:p.Asp166ArgfsTer7