Canonical Allele Identifier: CA2691805423

Gene: ENG

Linked Data

• gnomAD v4: 9-127815383-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815383A>T , CM000671.2:g.127815383A>T	GRCh38
NC_000009.11:g.130577662A>T , CM000671.1:g.130577662A>T	GRCh37
NC_000009.10:g.129617483A>T	NCBI36
NG_009551.1:g.44386T>A , LRG_589:g.44386T>A
NG_023245.1:g.17509A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*299T>A	ENSP00000479015.1:n.*299T>A
ENST00000373203.9:c.*299T>A MANE Select	ENSP00000362299.4:n.*299T>A
ENST00000344849.4:c.*534T>A	ENSP00000341917.3:n.*534T>A
ENST00000373203.8:c.*299T>A	ENSP00000362299.4:n.*299T>A
ENST00000480266.5:c.*299T>A	ENSP00000479015.1:n.*299T>A
NM_000118.3:c.*534T>A , LRG_589t1:c.*534T>A	NP_000109.1:n.*534T>A
NM_001114753.2:c.*299T>A , LRG_589t2:c.*299T>A	NP_001108225.1:n.*299T>A
NM_001278138.1:c.*299T>A	NP_001265067.1:n.*299T>A
NM_001114753.3:c.*299T>A MANE Select	NP_001108225.1:n.*299T>A
NM_001278138.2:c.*299T>A	NP_001265067.1:n.*299T>A