Canonical Allele Identifier: CA16612407
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407132
ClinVar RCV Id: RCV000756079 RCV002230338
dbSNP Id: rs1060501419
MyVariant Identifiers: chr9:g.130587166C>A (hg19) chr9:g.127824887C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824887C>A , CM000671.2:g.127824887C>A GRCh38
NC_000009.11:g.130587166C>A , CM000671.1:g.130587166C>A GRCh37
NC_000009.10:g.129626987C>A NCBI36
NG_009551.1:g.34882G>T , LRG_589:g.34882G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.358G>T ENSP00000479015.1:p.Glu120Ter
ENST00000373203.9:c.904G>T MANE Select ENSP00000362299.4:p.Glu302Ter
ENST00000344849.4:c.904G>T ENSP00000341917.3:p.Glu302Ter
ENST00000373203.8:c.904G>T ENSP00000362299.4:p.Glu302Ter
ENST00000480266.5:c.358G>T ENSP00000479015.1:p.Glu120Ter
NM_000118.3:c.904G>T , LRG_589t1:c.904G>T NP_000109.1:p.Glu302Ter
NM_001114753.2:c.904G>T , LRG_589t2:c.904G>T NP_001108225.1:p.Glu302Ter
NM_001278138.1:c.358G>T NP_001265067.1:p.Glu120Ter
NM_001114753.3:c.904G>T MANE Select NP_001108225.1:p.Glu302Ter
NM_001278138.2:c.358G>T NP_001265067.1:p.Glu120Ter
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