Canonical Allele Identifier: CA2691805142

Gene: ENG

Linked Data

• gnomAD v4: 9-127815137-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815137A>G , CM000671.2:g.127815137A>G	GRCh38
NC_000009.11:g.130577416A>G , CM000671.1:g.130577416A>G	GRCh37
NC_000009.10:g.129617237A>G	NCBI36
NG_009551.1:g.44632T>C , LRG_589:g.44632T>C
NG_023245.1:g.17263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*545T>C	ENSP00000479015.1:n.*545T>C
ENST00000373203.9:c.*545T>C MANE Select	ENSP00000362299.4:n.*545T>C
ENST00000344849.4:c.*780T>C	ENSP00000341917.3:n.*780T>C
ENST00000373203.8:c.*545T>C	ENSP00000362299.4:n.*545T>C
ENST00000480266.5:c.*545T>C	ENSP00000479015.1:n.*545T>C
NM_000118.3:c.*780T>C , LRG_589t1:c.*780T>C	NP_000109.1:n.*780T>C
NM_001114753.2:c.*545T>C , LRG_589t2:c.*545T>C	NP_001108225.1:n.*545T>C
NM_001278138.1:c.*545T>C	NP_001265067.1:n.*545T>C
NM_001114753.3:c.*545T>C MANE Select	NP_001108225.1:n.*545T>C
NM_001278138.2:c.*545T>C	NP_001265067.1:n.*545T>C