Canonical Allele Identifier: CA1879998959
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854385C= , CM000671.2:g.127854385C= GRCh38
NC_000009.11:g.130616664C= , CM000671.1:g.130616664C= GRCh37
NC_000009.10:g.129656485C= NCBI36
NG_009551.1:g.5384G= , LRG_589:g.5384G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.-30G= MANE Select ENSP00000362299.4:n.-30G=
ENST00000344849.4:c.-30G= ENSP00000341917.3:n.-30G=
ENST00000373203.8:c.-30G= ENSP00000362299.4:n.-30G=
NM_000118.3:c.-30G= , LRG_589t1:c.-30G= NP_000109.1:n.-30G=
NM_001114753.2:c.-30G= , LRG_589t2:c.-30G= NP_001108225.1:n.-30G=
NM_001114753.3:c.-30G= MANE Select NP_001108225.1:n.-30G=