Canonical Allele Identifier: CA2695211217
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824304del , CM000671.2:g.127824304del GRCh38
NC_000009.11:g.130586583del , CM000671.1:g.130586583del GRCh37
NC_000009.10:g.129626404del NCBI36
NG_009551.1:g.35466del , LRG_589:g.35466del

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.588+1del
ENST00000373203.9:c.1134+1del
ENST00000344849.4:c.1134+1del
ENST00000373203.8:c.1134+1del
ENST00000480266.5:c.588+1del
ENST00000486329.1:n.102+1del
NM_000118.3:c.1134+1del , LRG_589t1:c.1134+1del
NM_001114753.2:c.1134+1del , LRG_589t2:c.1134+1del
NM_001278138.1:c.588+1del
NM_001114753.3:c.1134+1del
NM_001278138.2:c.588+1del