Canonical Allele Identifier: CA1879989849

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819972_127819973delinsAC , CM000671.2:g.127819972_127819973delinsAC	GRCh38
NC_000009.11:g.130582251_130582252delinsAC , CM000671.1:g.130582251_130582252delinsAC	GRCh37
NC_000009.10:g.129622072_129622073delinsAC	NCBI36
NG_009551.1:g.39796_39797delinsGT , LRG_589:g.39796_39797delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.653_654delinsGT	ENSP00000479015.1:p.Gly218=
ENST00000373203.9:c.1199_1200delinsGT MANE Select	ENSP00000362299.4:p.Gly400=
ENST00000344849.4:c.1199_1200delinsGT	ENSP00000341917.3:p.Gly400=
ENST00000373203.8:c.1199_1200delinsGT	ENSP00000362299.4:p.Gly400=
ENST00000480266.5:c.653_654delinsGT	ENSP00000479015.1:p.Gly218=
ENST00000486329.1:n.167_168delinsGT
NM_000118.3:c.1199_1200delinsGT , LRG_589t1:c.1199_1200delinsGT	NP_000109.1:p.Gly400=
NM_001114753.2:c.1199_1200delinsGT , LRG_589t2:c.1199_1200delinsGT	NP_001108225.1:p.Gly400=
NM_001278138.1:c.653_654delinsGT	NP_001265067.1:p.Gly218=
NR_136302.1:n.1569-1223_1569-1222delinsAC
NM_001114753.3:c.1199_1200delinsGT MANE Select	NP_001108225.1:p.Gly400=
NM_001278138.2:c.653_654delinsGT	NP_001265067.1:p.Gly218=