Canonical Allele Identifier: CA1879972863
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824479_127824490delinsGTCACTGTGTGA , CM000671.2:g.127824479_127824490delinsGTCACTGTGTGA GRCh38
NC_000009.11:g.130586758_130586769delinsGTCACTGTGTGA , CM000671.1:g.130586758_130586769delinsGTCACTGTGTGA GRCh37
NC_000009.10:g.129626579_129626590delinsGTCACTGTGTGA NCBI36
NG_009551.1:g.35279_35290delinsTCACACAGTGAC , LRG_589:g.35279_35290delinsTCACACAGTGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.446-44_446-33delinsTCACACAGTGAC ENSP00000479015.1:n.446-44_446-33delinsTCACACAGTGAC
ENST00000373203.9:c.992-44_992-33delinsTCACACAGTGAC MANE Select ENSP00000362299.4:n.992-44_992-33delinsTCACACAGTGAC
ENST00000344849.4:c.992-44_992-33delinsTCACACAGTGAC ENSP00000341917.3:n.992-44_992-33delinsTCACACAGTGAC
ENST00000373203.8:c.992-44_992-33delinsTCACACAGTGAC ENSP00000362299.4:n.992-44_992-33delinsTCACACAGTGAC
ENST00000480266.5:c.446-44_446-33delinsTCACACAGTGAC ENSP00000479015.1:n.446-44_446-33delinsTCACACAGTGAC
NM_000118.3:c.992-44_992-33delinsTCACACAGTGAC , LRG_589t1:c.992-44_992-33delinsTCACACAGTGAC NP_000109.1:n.992-44_992-33delinsTCACACAGTGAC
NM_001114753.2:c.992-44_992-33delinsTCACACAGTGAC , LRG_589t2:c.992-44_992-33delinsTCACACAGTGAC NP_001108225.1:n.992-44_992-33delinsTCACACAGTGAC
NM_001278138.1:c.446-44_446-33delinsTCACACAGTGAC NP_001265067.1:n.446-44_446-33delinsTCACACAGTGAC
NM_001114753.3:c.992-44_992-33delinsTCACACAGTGAC MANE Select NP_001108225.1:n.992-44_992-33delinsTCACACAGTGAC
NM_001278138.2:c.446-44_446-33delinsTCACACAGTGAC NP_001265067.1:n.446-44_446-33delinsTCACACAGTGAC