Canonical Allele Identifier: CA1879998337

Gene: ENG

Linked Data

• dbSNP Id: rs1829091042

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854044_127854047dup , CM000671.2:g.127854044_127854047dup	GRCh38
NC_000009.11:g.130616323_130616326dup , CM000671.1:g.130616323_130616326dup	GRCh37
NC_000009.10:g.129656144_129656147dup	NCBI36
NG_009551.1:g.5723_5726dup , LRG_589:g.5723_5726dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.67+243_67+246dup MANE Select	ENSP00000362299.4:n.67+243_67+246dup
ENST00000344849.4:c.67+243_67+246dup	ENSP00000341917.3:n.67+243_67+246dup
ENST00000373203.8:c.67+243_67+246dup	ENSP00000362299.4:n.67+243_67+246dup
NM_000118.3:c.67+243_67+246dup , LRG_589t1:c.67+243_67+246dup	NP_000109.1:n.67+243_67+246dup
NM_001114753.2:c.67+243_67+246dup , LRG_589t2:c.67+243_67+246dup	NP_001108225.1:n.67+243_67+246dup
NM_001114753.3:c.67+243_67+246dup MANE Select	NP_001108225.1:n.67+243_67+246dup