Canonical Allele Identifier: CA1879989499
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127819879_127819880delinsCT , CM000671.2:g.127819879_127819880delinsCT GRCh38
NC_000009.11:g.130582158_130582159delinsCT , CM000671.1:g.130582158_130582159delinsCT GRCh37
NC_000009.10:g.129621979_129621980delinsCT NCBI36
NG_009551.1:g.39889_39890delinsAG , LRG_589:g.39889_39890delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.726+20_726+21delinsAG ENSP00000479015.1:n.726+20_726+21delinsAG...
ENST00000373203.9:c.1272+20_1272+21delinsAG MANE Select ENSP00000362299.4:n.1272+20_1272+21delins...
ENST00000344849.4:c.1272+20_1272+21delinsAG ENSP00000341917.3:n.1272+20_1272+21delins...
ENST00000373203.8:c.1272+20_1272+21delinsAG ENSP00000362299.4:n.1272+20_1272+21delins...
ENST00000480266.5:c.726+20_726+21delinsAG ENSP00000479015.1:n.726+20_726+21delinsAG...
ENST00000486329.1:n.240+20_240+21delinsAG
NM_000118.3:c.1272+20_1272+21delinsAG , LRG_589t1:c.1272+20_1272+21delinsAG NP_000109.1:n.1272+20_1272+21delinsAG
NM_001114753.2:c.1272+20_1272+21delinsAG , LRG_589t2:c.1272+20_1272+21delinsAG NP_001108225.1:n.1272+20_1272+21delinsAG
NM_001278138.1:c.726+20_726+21delinsAG NP_001265067.1:n.726+20_726+21delinsAG
NR_136302.1:n.1568+1168_1568+1169delinsCT
NM_001114753.3:c.1272+20_1272+21delinsAG MANE Select NP_001108225.1:n.1272+20_1272+21delinsAG
NM_001278138.2:c.726+20_726+21delinsAG NP_001265067.1:n.726+20_726+21delinsAG