Canonical Allele Identifier: CA1879974916

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825351C= , CM000671.2:g.127825351C=	GRCh38
NC_000009.11:g.130587630C= , CM000671.1:g.130587630C=	GRCh37
NC_000009.10:g.129627451C=	NCBI36
NG_009551.1:g.34418G= , LRG_589:g.34418G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.150G=	ENSP00000479015.1:p.Arg50=
ENST00000373203.9:c.696G= MANE Select	ENSP00000362299.4:p.Arg232=
ENST00000344849.4:c.696G=	ENSP00000341917.3:p.Arg232=
ENST00000373203.8:c.696G=	ENSP00000362299.4:p.Arg232=
ENST00000480266.5:c.150G=	ENSP00000479015.1:p.Arg50=
NM_000118.3:c.696G= , LRG_589t1:c.696G=	NP_000109.1:p.Arg232=
NM_001114753.2:c.696G= , LRG_589t2:c.696G=	NP_001108225.1:p.Arg232=
NM_001278138.1:c.150G=	NP_001265067.1:p.Arg50=
NM_001114753.3:c.696G= MANE Select	NP_001108225.1:p.Arg232=
NM_001278138.2:c.150G=	NP_001265067.1:p.Arg50=