Canonical Allele Identifier: CA2691805812

Gene: ENG

Linked Data

• gnomAD v4: 9-127815886-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815891del , CM000671.2:g.127815891del	GRCh38
NC_000009.11:g.130578170del , CM000671.1:g.130578170del	GRCh37
NC_000009.10:g.129617991del	NCBI36
NG_009551.1:g.43882del , LRG_589:g.43882del
NG_023245.1:g.18017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1306+56del	ENSP00000479015.1:n.1306+56del
ENST00000373203.9:c.1852+56del MANE Select	ENSP00000362299.4:n.1852+56del
ENST00000344849.4:c.*30del	ENSP00000341917.3:n.*30del
ENST00000373203.8:c.1852+56del	ENSP00000362299.4:n.1852+56del
ENST00000480266.5:c.1306+56del	ENSP00000479015.1:n.1306+56del
NM_000118.3:c.*30del , LRG_589t1:c.*30del	NP_000109.1:n.*30del
NM_001114753.2:c.1852+56del , LRG_589t2:c.1852+56del	NP_001108225.1:n.1852+56del
NM_001278138.1:c.1306+56del	NP_001265067.1:n.1306+56del
NM_001114753.3:c.1852+56del MANE Select	NP_001108225.1:n.1852+56del
NM_001278138.2:c.1306+56del	NP_001265067.1:n.1306+56del