Canonical Allele Identifier: CA2691806498

Gene: ENG

Linked Data

• gnomAD v4: 9-127819521-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819521C>T , CM000671.2:g.127819521C>T	GRCh38
NC_000009.11:g.130581800C>T , CM000671.1:g.130581800C>T	GRCh37
NC_000009.10:g.129621621C>T	NCBI36
NG_009551.1:g.40248G>A , LRG_589:g.40248G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.765+101G>A	ENSP00000479015.1:n.765+101G>A
ENST00000373203.9:c.1311+101G>A MANE Select	ENSP00000362299.4:n.1311+101G>A
ENST00000344849.4:c.1311+101G>A	ENSP00000341917.3:n.1311+101G>A
ENST00000373203.8:c.1311+101G>A	ENSP00000362299.4:n.1311+101G>A
ENST00000480266.5:c.765+101G>A	ENSP00000479015.1:n.765+101G>A
ENST00000486329.1:n.380G>A
NM_000118.3:c.1311+101G>A , LRG_589t1:c.1311+101G>A	NP_000109.1:n.1311+101G>A
NM_001114753.2:c.1311+101G>A , LRG_589t2:c.1311+101G>A	NP_001108225.1:n.1311+101G>A
NM_001278138.1:c.765+101G>A	NP_001265067.1:n.765+101G>A
NR_136302.1:n.1568+810C>T
NM_001114753.3:c.1311+101G>A MANE Select	NP_001108225.1:n.1311+101G>A
NM_001278138.2:c.765+101G>A	NP_001265067.1:n.765+101G>A