Canonical Allele Identifier: CA1879972722
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824414G= , CM000671.2:g.127824414G= GRCh38
NC_000009.11:g.130586693G= , CM000671.1:g.130586693G= GRCh37
NC_000009.10:g.129626514G= NCBI36
NG_009551.1:g.35355C= , LRG_589:g.35355C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.478C= ENSP00000479015.1:p.Gln160=
ENST00000373203.9:c.1024C= MANE Select ENSP00000362299.4:p.Gln342=
ENST00000344849.4:c.1024C= ENSP00000341917.3:p.Gln342=
ENST00000373203.8:c.1024C= ENSP00000362299.4:p.Gln342=
ENST00000480266.5:c.478C= ENSP00000479015.1:p.Gln160=
NM_000118.3:c.1024C= , LRG_589t1:c.1024C= NP_000109.1:p.Gln342=
NM_001114753.2:c.1024C= , LRG_589t2:c.1024C= NP_001108225.1:p.Gln342=
NM_001278138.1:c.478C= NP_001265067.1:p.Gln160=
NM_001114753.3:c.1024C= MANE Select NP_001108225.1:p.Gln342=
NM_001278138.2:c.478C= NP_001265067.1:p.Gln160=