Canonical Allele Identifier: CA1879998811

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854349G= , CM000671.2:g.127854349G=	GRCh38
NC_000009.11:g.130616628G= , CM000671.1:g.130616628G=	GRCh37
NC_000009.10:g.129656449G=	NCBI36
NG_009551.1:g.5420C= , LRG_589:g.5420C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373203.9:c.7C= MANE Select	ENSP00000362299.4:p.Arg3=
ENST00000344849.4:c.7C=	ENSP00000341917.3:p.Arg3=
ENST00000373203.8:c.7C=	ENSP00000362299.4:p.Arg3=
NM_000118.3:c.7C= , LRG_589t1:c.7C=	NP_000109.1:p.Arg3=
NM_001114753.2:c.7C= , LRG_589t2:c.7C=	NP_001108225.1:p.Arg3=
NM_001114753.3:c.7C= MANE Select	NP_001108225.1:p.Arg3=