Canonical Allele Identifier: CA1879977356
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127826536T= , CM000671.2:g.127826536T= GRCh38
NC_000009.11:g.130588815T= , CM000671.1:g.130588815T= GRCh37
NC_000009.10:g.129628636T= NCBI36
NG_009551.1:g.33233A= , LRG_589:g.33233A=

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.-50A= ENSP00000479015.1:n.-50A=
ENST00000373203.9:c.497A= MANE Select ENSP00000362299.4:p.Gln166=
ENST00000344849.4:c.497A= ENSP00000341917.3:p.Gln166=
ENST00000373203.8:c.497A= ENSP00000362299.4:p.Gln166=
ENST00000462196.1:n.397A=
ENST00000480266.5:c.-50A= ENSP00000479015.1:n.-50A=
NM_000118.3:c.497A= , LRG_589t1:c.497A= NP_000109.1:p.Gln166=
NM_001114753.2:c.497A= , LRG_589t2:c.497A= NP_001108225.1:p.Gln166=
NM_001278138.1:c.-50A= NP_001265067.1:n.-50A=
XR_001746952.2:n.82+1078T=
NM_001114753.3:c.497A= MANE Select NP_001108225.1:p.Gln166=
NM_001278138.2:c.-50A= NP_001265067.1:n.-50A=