Canonical Allele Identifier: CA1879981382

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815777C= , CM000671.2:g.127815777C=	GRCh38
NC_000009.11:g.130578056C= , CM000671.1:g.130578056C=	GRCh37
NC_000009.10:g.129617877C=	NCBI36
NG_009551.1:g.43992G= , LRG_589:g.43992G=
NG_023245.1:g.17903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1336G=	ENSP00000479015.1:p.Ala446=
ENST00000373203.9:c.1882G= MANE Select	ENSP00000362299.4:p.Ala628=
ENST00000344849.4:c.*140G=	ENSP00000341917.3:n.*140G=
ENST00000373203.8:c.1882G=	ENSP00000362299.4:p.Ala628=
ENST00000480266.5:c.1336G=	ENSP00000479015.1:p.Ala446=
NM_000118.3:c.*140G= , LRG_589t1:c.*140G=	NP_000109.1:n.*140G=
NM_001114753.2:c.1882G= , LRG_589t2:c.1882G=	NP_001108225.1:p.Ala628=
NM_001278138.1:c.1336G=	NP_001265067.1:p.Ala446=
NM_001114753.3:c.1882G= MANE Select	NP_001108225.1:p.Ala628=
NM_001278138.2:c.1336G=	NP_001265067.1:p.Ala446=