Canonical Allele Identifier: CA1879980248

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815261G= , CM000671.2:g.127815261G=	GRCh38
NC_000009.11:g.130577540G= , CM000671.1:g.130577540G=	GRCh37
NC_000009.10:g.129617361G=	NCBI36
NG_009551.1:g.44508C= , LRG_589:g.44508C=
NG_023245.1:g.17387G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*421C=	ENSP00000479015.1:n.*421C=
ENST00000373203.9:c.*421C= MANE Select	ENSP00000362299.4:n.*421C=
ENST00000344849.4:c.*656C=	ENSP00000341917.3:n.*656C=
ENST00000373203.8:c.*421C=	ENSP00000362299.4:n.*421C=
ENST00000480266.5:c.*421C=	ENSP00000479015.1:n.*421C=
NM_000118.3:c.*656C= , LRG_589t1:c.*656C=	NP_000109.1:n.*656C=
NM_001114753.2:c.*421C= , LRG_589t2:c.*421C=	NP_001108225.1:n.*421C=
NM_001278138.1:c.*421C=	NP_001265067.1:n.*421C=
NM_001114753.3:c.*421C= MANE Select	NP_001108225.1:n.*421C=
NM_001278138.2:c.*421C=	NP_001265067.1:n.*421C=