Canonical Allele Identifier: CA1879980356

Gene: ENG

Linked Data

• dbSNP Id: rs1830277867

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815315dup , CM000671.2:g.127815315dup	GRCh38
NC_000009.11:g.130577594dup , CM000671.1:g.130577594dup	GRCh37
NC_000009.10:g.129617415dup	NCBI36
NG_009551.1:g.44455dup , LRG_589:g.44455dup
NG_023245.1:g.17441dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*368dup	ENSP00000479015.1:n.*368dup
ENST00000373203.9:c.*368dup MANE Select	ENSP00000362299.4:n.*368dup
ENST00000344849.4:c.*603dup	ENSP00000341917.3:n.*603dup
ENST00000373203.8:c.*368dup	ENSP00000362299.4:n.*368dup
ENST00000480266.5:c.*368dup	ENSP00000479015.1:n.*368dup
NM_000118.3:c.*603dup , LRG_589t1:c.*603dup	NP_000109.1:n.*603dup
NM_001114753.2:c.*368dup , LRG_589t2:c.*368dup	NP_001108225.1:n.*368dup
NM_001278138.1:c.*368dup	NP_001265067.1:n.*368dup
NM_001114753.3:c.*368dup MANE Select	NP_001108225.1:n.*368dup
NM_001278138.2:c.*368dup	NP_001265067.1:n.*368dup