Canonical Allele Identifier: CA374986042
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127829751A>C , CM000671.2:g.127829751A>C GRCh38
NC_000009.11:g.130592030A>C , CM000671.1:g.130592030A>C GRCh37
NC_000009.10:g.129631851A>C NCBI36
NG_009551.1:g.30018T>G , LRG_589:g.30018T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.-251T>G ENSP00000479015.1:n.-251T>G
ENST00000373203.9:c.296T>G MANE Select ENSP00000362299.4:p.Leu99Arg
ENST00000344849.4:c.296T>G ENSP00000341917.3:p.Leu99Arg
ENST00000373203.8:c.296T>G ENSP00000362299.4:p.Leu99Arg
ENST00000462196.1:n.54T>G
ENST00000480266.5:c.-251T>G ENSP00000479015.1:n.-251T>G
NM_000118.3:c.296T>G , LRG_589t1:c.296T>G NP_000109.1:p.Leu99Arg
NM_001114753.2:c.296T>G , LRG_589t2:c.296T>G NP_001108225.1:p.Leu99Arg
NM_001278138.1:c.-251T>G NP_001265067.1:n.-251T>G
XR_001746952.2:n.83-2647A>C
NM_001114753.3:c.296T>G MANE Select NP_001108225.1:p.Leu99Arg
NM_001278138.2:c.-251T>G NP_001265067.1:n.-251T>G