Canonical Allele Identifier: CA1879989885

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819976_127819977delinsCT , CM000671.2:g.127819976_127819977delinsCT	GRCh38
NC_000009.11:g.130582255_130582256delinsCT , CM000671.1:g.130582255_130582256delinsCT	GRCh37
NC_000009.10:g.129622076_129622077delinsCT	NCBI36
NG_009551.1:g.39792_39793delinsAG , LRG_589:g.39792_39793delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.649_650delinsAG	ENSP00000479015.1:p.Arg217=
ENST00000373203.9:c.1195_1196delinsAG MANE Select	ENSP00000362299.4:p.Arg399=
ENST00000344849.4:c.1195_1196delinsAG	ENSP00000341917.3:p.Arg399=
ENST00000373203.8:c.1195_1196delinsAG	ENSP00000362299.4:p.Arg399=
ENST00000480266.5:c.649_650delinsAG	ENSP00000479015.1:p.Arg217=
ENST00000486329.1:n.163_164delinsAG
NM_000118.3:c.1195_1196delinsAG , LRG_589t1:c.1195_1196delinsAG	NP_000109.1:p.Arg399=
NM_001114753.2:c.1195_1196delinsAG , LRG_589t2:c.1195_1196delinsAG	NP_001108225.1:p.Arg399=
NM_001278138.1:c.649_650delinsAG	NP_001265067.1:p.Arg217=
NR_136302.1:n.1569-1219_1569-1218delinsCT
NM_001114753.3:c.1195_1196delinsAG MANE Select	NP_001108225.1:p.Arg399=
NM_001278138.2:c.649_650delinsAG	NP_001265067.1:p.Arg217=