Canonical Allele Identifier: CA374971731
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127815960T>A , CM000671.2:g.127815960T>A GRCh38
NC_000009.11:g.130578239T>A , CM000671.1:g.130578239T>A GRCh37
NC_000009.10:g.129618060T>A NCBI36
NG_009551.1:g.43809A>T , LRG_589:g.43809A>T
NG_023245.1:g.18086T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.1289A>T ENSP00000479015.1:p.Tyr430Phe
ENST00000373203.9:c.1835A>T MANE Select ENSP00000362299.4:p.Tyr612Phe
ENST00000344849.4:c.1835A>T ENSP00000341917.3:p.Tyr612Phe
ENST00000373203.8:c.1835A>T ENSP00000362299.4:p.Tyr612Phe
ENST00000480266.5:c.1289A>T ENSP00000479015.1:p.Tyr430Phe
NM_000118.3:c.1835A>T , LRG_589t1:c.1835A>T NP_000109.1:p.Tyr612Phe
NM_001114753.2:c.1835A>T , LRG_589t2:c.1835A>T NP_001108225.1:p.Tyr612Phe
NM_001278138.1:c.1289A>T NP_001265067.1:p.Tyr430Phe
NM_001114753.3:c.1835A>T MANE Select NP_001108225.1:p.Tyr612Phe
NM_001278138.2:c.1289A>T NP_001265067.1:p.Tyr430Phe