Canonical Allele Identifier: CA1879999476
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854753T= , CM000671.2:g.127854753T= GRCh38
NC_000009.11:g.130617032T= , CM000671.1:g.130617032T= GRCh37
NC_000009.10:g.129656853T= NCBI36
NG_009551.1:g.5016A= , LRG_589:g.5016A=

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.8:c.-398A= ENSP00000362299.4:n.-398A=
NM_000118.3:c.-398A= , LRG_589t1:c.-398A= NP_000109.1:n.-398A=
NM_001114753.2:c.-398A= , LRG_589t2:c.-398A= NP_001108225.1:n.-398A=