Canonical Allele Identifier: CA1139661221

Gene: ENG

Linked Data

• ClinVar Variation Id: 983209
• ClinVar RCV Id: RCV001263083
• dbSNP Id: rs1830620247

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826541del , CM000671.2:g.127826541del	GRCh38
NC_000009.11:g.130588820del , CM000671.1:g.130588820del	GRCh37
NC_000009.10:g.129628641del	NCBI36
NG_009551.1:g.33232del , LRG_589:g.33232del

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-51del	ENSP00000479015.1:n.-51del
ENST00000373203.9:c.496del MANE Select	ENSP00000362299.4:p.Gln166ArgfsTer?
ENST00000344849.4:c.496del	ENSP00000341917.3:p.Gln166ArgfsTer?
ENST00000373203.8:c.496del	ENSP00000362299.4:p.Gln166ArgfsTer?
ENST00000462196.1:n.396del
ENST00000480266.5:c.-51del	ENSP00000479015.1:n.-51del
NM_000118.3:c.496del , LRG_589t1:c.496del	NP_000109.1:p.Gln166ArgfsTer?
NM_001114753.2:c.496del , LRG_589t2:c.496del	NP_001108225.1:p.Gln166ArgfsTer?
NM_001278138.1:c.-51del	NP_001265067.1:n.-51del
XR_001746952.2:n.82+1083del
NM_001114753.3:c.496del MANE Select	NP_001108225.1:p.Gln166ArgfsTer?
NM_001278138.2:c.-51del	NP_001265067.1:n.-51del