Canonical Allele Identifier: CA2691806670

Gene: ENG

Linked Data

• gnomAD v4: 9-127820094-C-CAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820095_127820096insGAGA , CM000671.2:g.127820095_127820096insGAGA	GRCh38
NC_000009.11:g.130582374_130582375insGAGA , CM000671.1:g.130582374_130582375insGAGA	GRCh37
NC_000009.10:g.129622195_129622196insGAGA	NCBI36
NG_009551.1:g.39674_39675insCTCT , LRG_589:g.39674_39675insCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-58_589-57insCTCT	ENSP00000479015.1:n.589-58_589-57insCTCT
ENST00000373203.9:c.1135-58_1135-57insCTCT MANE Select	ENSP00000362299.4:n.1135-58_1135-57insCTCT
ENST00000344849.4:c.1135-58_1135-57insCTCT	ENSP00000341917.3:n.1135-58_1135-57insCTCT
ENST00000373203.8:c.1135-58_1135-57insCTCT	ENSP00000362299.4:n.1135-58_1135-57insCTCT
ENST00000480266.5:c.589-58_589-57insCTCT	ENSP00000479015.1:n.589-58_589-57insCTCT
ENST00000486329.1:n.103-58_103-57insCTCT
NM_000118.3:c.1135-58_1135-57insCTCT , LRG_589t1:c.1135-58_1135-57insCTCT	NP_000109.1:n.1135-58_1135-57insCTCT
NM_001114753.2:c.1135-58_1135-57insCTCT , LRG_589t2:c.1135-58_1135-57insCTCT	NP_001108225.1:n.1135-58_1135-57insCTCT
NM_001278138.1:c.589-58_589-57insCTCT	NP_001265067.1:n.589-58_589-57insCTCT
NR_136302.1:n.1569-1100_1569-1099insGAGA
NM_001114753.3:c.1135-58_1135-57insCTCT MANE Select	NP_001108225.1:n.1135-58_1135-57insCTCT
NM_001278138.2:c.589-58_589-57insCTCT	NP_001265067.1:n.589-58_589-57insCTCT