Canonical Allele Identifier: CA1879972636
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824380T= , CM000671.2:g.127824380T= GRCh38
NC_000009.11:g.130586659T= , CM000671.1:g.130586659T= GRCh37
NC_000009.10:g.129626480T= NCBI36
NG_009551.1:g.35389A= , LRG_589:g.35389A=

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.512A= ENSP00000479015.1:p.Glu171=
ENST00000373203.9:c.1058A= MANE Select ENSP00000362299.4:p.Glu353=
ENST00000344849.4:c.1058A= ENSP00000341917.3:p.Glu353=
ENST00000373203.8:c.1058A= ENSP00000362299.4:p.Glu353=
ENST00000480266.5:c.512A= ENSP00000479015.1:p.Glu171=
ENST00000486329.1:n.26A=
NM_000118.3:c.1058A= , LRG_589t1:c.1058A= NP_000109.1:p.Glu353=
NM_001114753.2:c.1058A= , LRG_589t2:c.1058A= NP_001108225.1:p.Glu353=
NM_001278138.1:c.512A= NP_001265067.1:p.Glu171=
NM_001114753.3:c.1058A= MANE Select NP_001108225.1:p.Glu353=
NM_001278138.2:c.512A= NP_001265067.1:p.Glu171=