Canonical Allele Identifier: CA2691806693

Gene: ENG

Linked Data

• gnomAD v4: 9-127820115-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820118_127820119dup , CM000671.2:g.127820118_127820119dup	GRCh38
NC_000009.11:g.130582397_130582398dup , CM000671.1:g.130582397_130582398dup	GRCh37
NC_000009.10:g.129622218_129622219dup	NCBI36
NG_009551.1:g.39652_39653dup , LRG_589:g.39652_39653dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-80_589-79dup	ENSP00000479015.1:n.589-80_589-79dup
ENST00000373203.9:c.1135-80_1135-79dup MANE Select	ENSP00000362299.4:n.1135-80_1135-79dup
ENST00000344849.4:c.1135-80_1135-79dup	ENSP00000341917.3:n.1135-80_1135-79dup
ENST00000373203.8:c.1135-80_1135-79dup	ENSP00000362299.4:n.1135-80_1135-79dup
ENST00000480266.5:c.589-80_589-79dup	ENSP00000479015.1:n.589-80_589-79dup
ENST00000486329.1:n.103-80_103-79dup
NM_000118.3:c.1135-80_1135-79dup , LRG_589t1:c.1135-80_1135-79dup	NP_000109.1:n.1135-80_1135-79dup
NM_001114753.2:c.1135-80_1135-79dup , LRG_589t2:c.1135-80_1135-79dup	NP_001108225.1:n.1135-80_1135-79dup
NM_001278138.1:c.589-80_589-79dup	NP_001265067.1:n.589-80_589-79dup
NR_136302.1:n.1569-1077_1569-1076dup
NM_001114753.3:c.1135-80_1135-79dup MANE Select	NP_001108225.1:n.1135-80_1135-79dup
NM_001278138.2:c.589-80_589-79dup	NP_001265067.1:n.589-80_589-79dup