Canonical Allele Identifier: CA1879980208
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127815242G= , CM000671.2:g.127815242G= GRCh38
NC_000009.11:g.130577521G= , CM000671.1:g.130577521G= GRCh37
NC_000009.10:g.129617342G= NCBI36
NG_009551.1:g.44527C= , LRG_589:g.44527C=
NG_023245.1:g.17368G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.*440C= ENSP00000479015.1:n.*440C=
ENST00000373203.9:c.*440C= MANE Select ENSP00000362299.4:n.*440C=
ENST00000344849.4:c.*675C= ENSP00000341917.3:n.*675C=
ENST00000373203.8:c.*440C= ENSP00000362299.4:n.*440C=
ENST00000480266.5:c.*440C= ENSP00000479015.1:n.*440C=
NM_000118.3:c.*675C= , LRG_589t1:c.*675C= NP_000109.1:n.*675C=
NM_001114753.2:c.*440C= , LRG_589t2:c.*440C= NP_001108225.1:n.*440C=
NM_001278138.1:c.*440C= NP_001265067.1:n.*440C=
NM_001114753.3:c.*440C= MANE Select NP_001108225.1:n.*440C=
NM_001278138.2:c.*440C= NP_001265067.1:n.*440C=