Canonical Allele Identifier: CA2697558068

Gene: ENG

Linked Data

• ClinVar Variation Id: 2723947
• ClinVar RCV Id: RCV003595376

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819898dup , CM000671.2:g.127819898dup	GRCh38
NC_000009.11:g.130582177dup , CM000671.1:g.130582177dup	GRCh37
NC_000009.10:g.129621998dup	NCBI36
NG_009551.1:g.39871dup , LRG_589:g.39871dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.726+2dup	ENSP00000479015.1:n.726+2dup
ENST00000373203.9:c.1272+2dup MANE Select	ENSP00000362299.4:n.1272+2dup
ENST00000344849.4:c.1272+2dup	ENSP00000341917.3:n.1272+2dup
ENST00000373203.8:c.1272+2dup	ENSP00000362299.4:n.1272+2dup
ENST00000480266.5:c.726+2dup	ENSP00000479015.1:n.726+2dup
ENST00000486329.1:n.240+2dup
NM_000118.3:c.1272+2dup , LRG_589t1:c.1272+2dup	NP_000109.1:n.1272+2dup
NM_001114753.2:c.1272+2dup , LRG_589t2:c.1272+2dup	NP_001108225.1:n.1272+2dup
NM_001278138.1:c.726+2dup	NP_001265067.1:n.726+2dup
NR_136302.1:n.1568+1187dup
NM_001114753.3:c.1272+2dup MANE Select	NP_001108225.1:n.1272+2dup
NM_001278138.2:c.726+2dup	NP_001265067.1:n.726+2dup