Canonical Allele Identifier: CA1879977647

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826646C= , CM000671.2:g.127826646C=	GRCh38
NC_000009.11:g.130588925C= , CM000671.1:g.130588925C=	GRCh37
NC_000009.10:g.129628746C=	NCBI36
NG_009551.1:g.33123G= , LRG_589:g.33123G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-160G=	ENSP00000479015.1:n.-160G=
ENST00000373203.9:c.387G= MANE Select	ENSP00000362299.4:p.Glu129=
ENST00000344849.4:c.387G=	ENSP00000341917.3:p.Glu129=
ENST00000373203.8:c.387G=	ENSP00000362299.4:p.Glu129=
ENST00000462196.1:n.287G=
ENST00000480266.5:c.-160G=	ENSP00000479015.1:n.-160G=
NM_000118.3:c.387G= , LRG_589t1:c.387G=	NP_000109.1:p.Glu129=
NM_001114753.2:c.387G= , LRG_589t2:c.387G=	NP_001108225.1:p.Glu129=
NM_001278138.1:c.-160G=	NP_001265067.1:n.-160G=
XR_001746952.2:n.82+1188C=
NM_001114753.3:c.387G= MANE Select	NP_001108225.1:p.Glu129=
NM_001278138.2:c.-160G=	NP_001265067.1:n.-160G=