Canonical Allele Identifier: CA1879998715

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854316_127854317delinsGC , CM000671.2:g.127854316_127854317delinsGC	GRCh38
NC_000009.11:g.130616595_130616596delinsGC , CM000671.1:g.130616595_130616596delinsGC	GRCh37
NC_000009.10:g.129656416_129656417delinsGC	NCBI36
NG_009551.1:g.5452_5453delinsGC , LRG_589:g.5452_5453delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.39_40delinsGC MANE Select	ENSP00000362299.4:p.Leu13=
ENST00000344849.4:c.39_40delinsGC	ENSP00000341917.3:p.Leu13=
ENST00000373203.8:c.39_40delinsGC	ENSP00000362299.4:p.Leu13=
NM_000118.3:c.39_40delinsGC , LRG_589t1:c.39_40delinsGC	NP_000109.1:p.Leu13=
NM_001114753.2:c.39_40delinsGC , LRG_589t2:c.39_40delinsGC	NP_001108225.1:p.Leu13=
NM_001114753.3:c.39_40delinsGC MANE Select	NP_001108225.1:p.Leu13=