Canonical Allele Identifier: CA1879980324

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815292A= , CM000671.2:g.127815292A=	GRCh38
NC_000009.11:g.130577571A= , CM000671.1:g.130577571A=	GRCh37
NC_000009.10:g.129617392A=	NCBI36
NG_009551.1:g.44477T= , LRG_589:g.44477T=
NG_023245.1:g.17418A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*390T=	ENSP00000479015.1:n.*390T=
ENST00000373203.9:c.*390T= MANE Select	ENSP00000362299.4:n.*390T=
ENST00000344849.4:c.*625T=	ENSP00000341917.3:n.*625T=
ENST00000373203.8:c.*390T=	ENSP00000362299.4:n.*390T=
ENST00000480266.5:c.*390T=	ENSP00000479015.1:n.*390T=
NM_000118.3:c.*625T= , LRG_589t1:c.*625T=	NP_000109.1:n.*625T=
NM_001114753.2:c.*390T= , LRG_589t2:c.*390T=	NP_001108225.1:n.*390T=
NM_001278138.1:c.*390T=	NP_001265067.1:n.*390T=
NM_001114753.3:c.*390T= MANE Select	NP_001108225.1:n.*390T=
NM_001278138.2:c.*390T=	NP_001265067.1:n.*390T=