Canonical Allele Identifier: CA1879980384

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815333T= , CM000671.2:g.127815333T=	GRCh38
NC_000009.11:g.130577612T= , CM000671.1:g.130577612T=	GRCh37
NC_000009.10:g.129617433T=	NCBI36
NG_009551.1:g.44436A= , LRG_589:g.44436A=
NG_023245.1:g.17459T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*349A=	ENSP00000479015.1:n.*349A=
ENST00000373203.9:c.*349A= MANE Select	ENSP00000362299.4:n.*349A=
ENST00000344849.4:c.*584A=	ENSP00000341917.3:n.*584A=
ENST00000373203.8:c.*349A=	ENSP00000362299.4:n.*349A=
ENST00000480266.5:c.*349A=	ENSP00000479015.1:n.*349A=
NM_000118.3:c.*584A= , LRG_589t1:c.*584A=	NP_000109.1:n.*584A=
NM_001114753.2:c.*349A= , LRG_589t2:c.*349A=	NP_001108225.1:n.*349A=
NM_001278138.1:c.*349A=	NP_001265067.1:n.*349A=
NM_001114753.3:c.*349A= MANE Select	NP_001108225.1:n.*349A=
NM_001278138.2:c.*349A=	NP_001265067.1:n.*349A=