Canonical Allele Identifier: CA2691809007

Gene: ENG

Linked Data

• gnomAD v4: 9-127825070-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825074del , CM000671.2:g.127825074del	GRCh38
NC_000009.11:g.130587353del , CM000671.1:g.130587353del	GRCh37
NC_000009.10:g.129627174del	NCBI36
NG_009551.1:g.34698del , LRG_589:g.34698del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.271-97del	ENSP00000479015.1:n.271-97del
ENST00000373203.9:c.817-97del MANE Select	ENSP00000362299.4:n.817-97del
ENST00000344849.4:c.817-97del	ENSP00000341917.3:n.817-97del
ENST00000373203.8:c.817-97del	ENSP00000362299.4:n.817-97del
ENST00000480266.5:c.271-97del	ENSP00000479015.1:n.271-97del
NM_000118.3:c.817-97del , LRG_589t1:c.817-97del	NP_000109.1:n.817-97del
NM_001114753.2:c.817-97del , LRG_589t2:c.817-97del	NP_001108225.1:n.817-97del
NM_001278138.1:c.271-97del	NP_001265067.1:n.271-97del
NM_001114753.3:c.817-97del MANE Select	NP_001108225.1:n.817-97del
NM_001278138.2:c.271-97del	NP_001265067.1:n.271-97del