Canonical Allele Identifier: CA1879998781
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854347G= , CM000671.2:g.127854347G= GRCh38
NC_000009.11:g.130616626G= , CM000671.1:g.130616626G= GRCh37
NC_000009.10:g.129656447G= NCBI36
NG_009551.1:g.5422C= , LRG_589:g.5422C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.9C= MANE Select ENSP00000362299.4:p.Arg3=
ENST00000344849.4:c.9C= ENSP00000341917.3:p.Arg3=
ENST00000373203.8:c.9C= ENSP00000362299.4:p.Arg3=
NM_000118.3:c.9C= , LRG_589t1:c.9C= NP_000109.1:p.Arg3=
NM_001114753.2:c.9C= , LRG_589t2:c.9C= NP_001108225.1:p.Arg3=
NM_001114753.3:c.9C= MANE Select NP_001108225.1:p.Arg3=