Canonical Allele Identifier: CA2691805849
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127815928del , CM000671.2:g.127815928del GRCh38
NC_000009.11:g.130578207del , CM000671.1:g.130578207del GRCh37
NC_000009.10:g.129618028del NCBI36
NG_009551.1:g.43845del , LRG_589:g.43845del
NG_023245.1:g.18054del

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1306+19del ENSP00000479015.1:n.1306+19del
ENST00000373203.9:c.1852+19del MANE Select ENSP00000362299.4:n.1852+19del
ENST00000344849.4:c.1871del ENSP00000341917.3:p.Pro624HisfsTer16
ENST00000373203.8:c.1852+19del ENSP00000362299.4:n.1852+19del
ENST00000480266.5:c.1306+19del ENSP00000479015.1:n.1306+19del
NM_000118.3:c.1871del , LRG_589t1:c.1871del NP_000109.1:p.Pro624HisfsTer16
NM_001114753.2:c.1852+19del , LRG_589t2:c.1852+19del NP_001108225.1:n.1852+19del
NM_001278138.1:c.1306+19del NP_001265067.1:n.1306+19del
NM_001114753.3:c.1852+19del MANE Select NP_001108225.1:n.1852+19del
NM_001278138.2:c.1306+19del NP_001265067.1:n.1306+19del