Canonical Allele Identifier: CA374974252
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127818178T>A , CM000671.2:g.127818178T>A GRCh38
NC_000009.11:g.130580457T>A , CM000671.1:g.130580457T>A GRCh37
NC_000009.10:g.129620278T>A NCBI36
NG_009551.1:g.41591A>T , LRG_589:g.41591A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1082A>T ENSP00000479015.1:p.Lys361Ile
ENST00000373203.9:c.1628A>T MANE Select ENSP00000362299.4:p.Lys543Ile
ENST00000344849.4:c.1628A>T ENSP00000341917.3:p.Lys543Ile
ENST00000373203.8:c.1628A>T ENSP00000362299.4:p.Lys543Ile
ENST00000480266.5:c.1082A>T ENSP00000479015.1:p.Lys361Ile
NM_000118.3:c.1628A>T , LRG_589t1:c.1628A>T NP_000109.1:p.Lys543Ile
NM_001114753.2:c.1628A>T , LRG_589t2:c.1628A>T NP_001108225.1:p.Lys543Ile
NM_001278138.1:c.1082A>T NP_001265067.1:p.Lys361Ile
NR_136302.1:n.1378-133T>A
NM_001114753.3:c.1628A>T MANE Select NP_001108225.1:p.Lys543Ile
NM_001278138.2:c.1082A>T NP_001265067.1:p.Lys361Ile