Canonical Allele Identifier: CA1879980129
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127815204C= , CM000671.2:g.127815204C= GRCh38
NC_000009.11:g.130577483C= , CM000671.1:g.130577483C= GRCh37
NC_000009.10:g.129617304C= NCBI36
NG_009551.1:g.44565G= , LRG_589:g.44565G=
NG_023245.1:g.17330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.*478G= ENSP00000479015.1:n.*478G=
ENST00000373203.9:c.*478G= MANE Select ENSP00000362299.4:n.*478G=
ENST00000344849.4:c.*713G= ENSP00000341917.3:n.*713G=
ENST00000373203.8:c.*478G= ENSP00000362299.4:n.*478G=
ENST00000480266.5:c.*478G= ENSP00000479015.1:n.*478G=
NM_000118.3:c.*713G= , LRG_589t1:c.*713G= NP_000109.1:n.*713G=
NM_001114753.2:c.*478G= , LRG_589t2:c.*478G= NP_001108225.1:n.*478G=
NM_001278138.1:c.*478G= NP_001265067.1:n.*478G=
NM_001114753.3:c.*478G= MANE Select NP_001108225.1:n.*478G=
NM_001278138.2:c.*478G= NP_001265067.1:n.*478G=