Canonical Allele Identifier: CA1139659930
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 960260
ClinVar RCV Id: RCV001233754
dbSNP Id: rs1830377451

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127818182dup , CM000671.2:g.127818182dup GRCh38
NC_000009.11:g.130580461dup , CM000671.1:g.130580461dup GRCh37
NC_000009.10:g.129620282dup NCBI36
NG_009551.1:g.41589dup , LRG_589:g.41589dup

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1080dup ENSP00000479015.1:p.Lys361GlnfsTer24
ENST00000373203.9:c.1626dup MANE Select ENSP00000362299.4:p.Lys543GlnfsTer24
ENST00000344849.4:c.1626dup ENSP00000341917.3:p.Lys543GlnfsTer24
ENST00000373203.8:c.1626dup ENSP00000362299.4:p.Lys543GlnfsTer24
ENST00000480266.5:c.1080dup ENSP00000479015.1:p.Lys361GlnfsTer24
NM_000118.3:c.1626dup , LRG_589t1:c.1626dup NP_000109.1:p.Lys543GlnfsTer24
NM_001114753.2:c.1626dup , LRG_589t2:c.1626dup NP_001108225.1:p.Lys543GlnfsTer24
NM_001278138.1:c.1080dup NP_001265067.1:p.Lys361GlnfsTer24
NR_136302.1:n.1378-129dup
NM_001114753.3:c.1626dup MANE Select NP_001108225.1:p.Lys543GlnfsTer24
NM_001278138.2:c.1080dup NP_001265067.1:p.Lys361GlnfsTer24