Canonical Allele Identifier: CA2691805127

Gene: ENG

Linked Data

• gnomAD v4: 9-127815120-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815120T>C , CM000671.2:g.127815120T>C	GRCh38
NC_000009.11:g.130577399T>C , CM000671.1:g.130577399T>C	GRCh37
NC_000009.10:g.129617220T>C	NCBI36
NG_009551.1:g.44649A>G , LRG_589:g.44649A>G
NG_023245.1:g.17246T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*562A>G	ENSP00000479015.1:n.*562A>G
ENST00000373203.9:c.*562A>G MANE Select	ENSP00000362299.4:n.*562A>G
ENST00000344849.4:c.*797A>G	ENSP00000341917.3:n.*797A>G
ENST00000373203.8:c.*562A>G	ENSP00000362299.4:n.*562A>G
ENST00000480266.5:c.*562A>G	ENSP00000479015.1:n.*562A>G
NM_000118.3:c.*797A>G , LRG_589t1:c.*797A>G	NP_000109.1:n.*797A>G
NM_001114753.2:c.*562A>G , LRG_589t2:c.*562A>G	NP_001108225.1:n.*562A>G
NM_001278138.1:c.*562A>G	NP_001265067.1:n.*562A>G
NM_001114753.3:c.*562A>G MANE Select	NP_001108225.1:n.*562A>G
NM_001278138.2:c.*562A>G	NP_001265067.1:n.*562A>G