Canonical Allele Identifier: CA374989621
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854327A>T , CM000671.2:g.127854327A>T GRCh38
NC_000009.11:g.130616606A>T , CM000671.1:g.130616606A>T GRCh37
NC_000009.10:g.129656427A>T NCBI36
NG_009551.1:g.5442T>A , LRG_589:g.5442T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.29T>A MANE Select ENSP00000362299.4:p.Val10Asp
ENST00000344849.4:c.29T>A ENSP00000341917.3:p.Val10Asp
ENST00000373203.8:c.29T>A ENSP00000362299.4:p.Val10Asp
NM_000118.3:c.29T>A , LRG_589t1:c.29T>A NP_000109.1:p.Val10Asp
NM_001114753.2:c.29T>A , LRG_589t2:c.29T>A NP_001108225.1:p.Val10Asp
NM_001114753.3:c.29T>A MANE Select NP_001108225.1:p.Val10Asp