Canonical Allele Identifier: CA1879999087
Gene: ENG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854475C= , CM000671.2:g.127854475C= GRCh38
NC_000009.11:g.130616754C= , CM000671.1:g.130616754C= GRCh37
NC_000009.10:g.129656575C= NCBI36
NG_009551.1:g.5294G= , LRG_589:g.5294G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.-120G= MANE Select ENSP00000362299.4:n.-120G=
ENST00000344849.4:c.-120G= ENSP00000341917.3:n.-120G=
ENST00000373203.8:c.-120G= ENSP00000362299.4:n.-120G=
NM_000118.3:c.-120G= , LRG_589t1:c.-120G= NP_000109.1:n.-120G=
NM_001114753.2:c.-120G= , LRG_589t2:c.-120G= NP_001108225.1:n.-120G=
NM_001114753.3:c.-120G= MANE Select NP_001108225.1:n.-120G=
Search 100 bp 5'
Search 100 bp 3'