Canonical Allele Identifier: CA1139661202
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127823973_127830053del , CM000671.2:g.127823973_127830053del GRCh38
NC_000009.11:g.130586252_130592332del , CM000671.1:g.130586252_130592332del GRCh37
NC_000009.10:g.129626073_129632153del NCBI36
NG_009551.1:g.29716_35796del , LRG_589:g.29716_35796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.-327-226_588+331del
ENST00000373203.9:c.220-226_1134+331del
ENST00000344849.4:c.220-226_1134+331del
ENST00000373203.8:c.220-226_1134+331del
ENST00000480266.5:c.-327-226_588+331del
NM_000118.3:c.220-226_1134+331del , LRG_589t1:c.220-226_1134+331del
NM_001114753.2:c.220-226_1134+331del , LRG_589t2:c.220-226_1134+331del
NM_001278138.1:c.-327-226_588+331del
NM_001114753.3:c.220-226_1134+331del
NM_001278138.2:c.-327-226_588+331del