Canonical Allele Identifier: CA1879998988

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854415G= , CM000671.2:g.127854415G=	GRCh38
NC_000009.11:g.130616694G= , CM000671.1:g.130616694G=	GRCh37
NC_000009.10:g.129656515G=	NCBI36
NG_009551.1:g.5354C= , LRG_589:g.5354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.-60C= MANE Select	ENSP00000362299.4:n.-60C=
ENST00000344849.4:c.-60C=	ENSP00000341917.3:n.-60C=
ENST00000373203.8:c.-60C=	ENSP00000362299.4:n.-60C=
NM_000118.3:c.-60C= , LRG_589t1:c.-60C=	NP_000109.1:n.-60C=
NM_001114753.2:c.-60C= , LRG_589t2:c.-60C=	NP_001108225.1:n.-60C=
NM_001114753.3:c.-60C= MANE Select	NP_001108225.1:n.-60C=