Canonical Allele Identifier: CA2691809032

Gene: ENG

Linked Data

• gnomAD v4: 9-127825109-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825109C>A , CM000671.2:g.127825109C>A	GRCh38
NC_000009.11:g.130587388C>A , CM000671.1:g.130587388C>A	GRCh37
NC_000009.10:g.129627209C>A	NCBI36
NG_009551.1:g.34660G>T , LRG_589:g.34660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.270+122G>T	ENSP00000479015.1:n.270+122G>T
ENST00000373203.9:c.816+122G>T MANE Select	ENSP00000362299.4:n.816+122G>T
ENST00000344849.4:c.816+122G>T	ENSP00000341917.3:n.816+122G>T
ENST00000373203.8:c.816+122G>T	ENSP00000362299.4:n.816+122G>T
ENST00000480266.5:c.270+122G>T	ENSP00000479015.1:n.270+122G>T
NM_000118.3:c.816+122G>T , LRG_589t1:c.816+122G>T	NP_000109.1:n.816+122G>T
NM_001114753.2:c.816+122G>T , LRG_589t2:c.816+122G>T	NP_001108225.1:n.816+122G>T
NM_001278138.1:c.270+122G>T	NP_001265067.1:n.270+122G>T
NM_001114753.3:c.816+122G>T MANE Select	NP_001108225.1:n.816+122G>T
NM_001278138.2:c.270+122G>T	NP_001265067.1:n.270+122G>T