Canonical Allele Identifier: CA1879998149
Gene: ENG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127853880T= , CM000671.2:g.127853880T= GRCh38
NC_000009.11:g.130616159T= , CM000671.1:g.130616159T= GRCh37
NC_000009.10:g.129655980T= NCBI36
NG_009551.1:g.5889A= , LRG_589:g.5889A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.67+409A= MANE Select ENSP00000362299.4:n.67+409A=
ENST00000344849.4:c.67+409A= ENSP00000341917.3:n.67+409A=
ENST00000373203.8:c.67+409A= ENSP00000362299.4:n.67+409A=
NM_000118.3:c.67+409A= , LRG_589t1:c.67+409A= NP_000109.1:n.67+409A=
NM_001114753.2:c.67+409A= , LRG_589t2:c.67+409A= NP_001108225.1:n.67+409A=
NM_001114753.3:c.67+409A= MANE Select NP_001108225.1:n.67+409A=
Search 100 bp 5'
Search 100 bp 3'