Canonical Allele Identifier: CA2691809000

Gene: ENG

Linked Data

• gnomAD v4: 9-127825059-G-GTCCTGCTGTGTCCCCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825068_127825084dup , CM000671.2:g.127825068_127825084dup	GRCh38
NC_000009.11:g.130587347_130587363dup , CM000671.1:g.130587347_130587363dup	GRCh37
NC_000009.10:g.129627168_129627184dup	NCBI36
NG_009551.1:g.34693_34709dup , LRG_589:g.34693_34709dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.271-102_271-86dup	ENSP00000479015.1:n.271-102_271-86dup
ENST00000373203.9:c.817-102_817-86dup MANE Select	ENSP00000362299.4:n.817-102_817-86dup
ENST00000344849.4:c.817-102_817-86dup	ENSP00000341917.3:n.817-102_817-86dup
ENST00000373203.8:c.817-102_817-86dup	ENSP00000362299.4:n.817-102_817-86dup
ENST00000480266.5:c.271-102_271-86dup	ENSP00000479015.1:n.271-102_271-86dup
NM_000118.3:c.817-102_817-86dup , LRG_589t1:c.817-102_817-86dup	NP_000109.1:n.817-102_817-86dup
NM_001114753.2:c.817-102_817-86dup , LRG_589t2:c.817-102_817-86dup	NP_001108225.1:n.817-102_817-86dup
NM_001278138.1:c.271-102_271-86dup	NP_001265067.1:n.271-102_271-86dup
NM_001114753.3:c.817-102_817-86dup MANE Select	NP_001108225.1:n.817-102_817-86dup
NM_001278138.2:c.271-102_271-86dup	NP_001265067.1:n.271-102_271-86dup