Canonical Allele Identifier: CA1879977453

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826587C= , CM000671.2:g.127826587C=	GRCh38
NC_000009.11:g.130588866C= , CM000671.1:g.130588866C=	GRCh37
NC_000009.10:g.129628687C=	NCBI36
NG_009551.1:g.33182G= , LRG_589:g.33182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-101G=	ENSP00000479015.1:n.-101G=
ENST00000373203.9:c.446G= MANE Select	ENSP00000362299.4:p.Trp149=
ENST00000344849.4:c.446G=	ENSP00000341917.3:p.Trp149=
ENST00000373203.8:c.446G=	ENSP00000362299.4:p.Trp149=
ENST00000462196.1:n.346G=
ENST00000480266.5:c.-101G=	ENSP00000479015.1:n.-101G=
NM_000118.3:c.446G= , LRG_589t1:c.446G=	NP_000109.1:p.Trp149=
NM_001114753.2:c.446G= , LRG_589t2:c.446G=	NP_001108225.1:p.Trp149=
NM_001278138.1:c.-101G=	NP_001265067.1:n.-101G=
XR_001746952.2:n.82+1129C=
NM_001114753.3:c.446G= MANE Select	NP_001108225.1:p.Trp149=
NM_001278138.2:c.-101G=	NP_001265067.1:n.-101G=