Canonical Allele Identifier: CA2842474670

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854332dup , CM000671.2:g.127854332dup	GRCh38
NC_000009.11:g.130616611dup , CM000671.1:g.130616611dup	GRCh37
NC_000009.10:g.129656432dup	NCBI36
NG_009551.1:g.5438dup , LRG_589:g.5438dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.25dup MANE Select	ENSP00000362299.4:p.Ala9GlyfsTer23
ENST00000344849.4:c.25dup	ENSP00000341917.3:p.Ala9GlyfsTer23
ENST00000373203.8:c.25dup	ENSP00000362299.4:p.Ala9GlyfsTer23
NM_000118.3:c.25dup , LRG_589t1:c.25dup	NP_000109.1:p.Ala9GlyfsTer23
NM_001114753.2:c.25dup , LRG_589t2:c.25dup	NP_001108225.1:p.Ala9GlyfsTer23
NM_001114753.3:c.25dup MANE Select	NP_001108225.1:p.Ala9GlyfsTer23