Canonical Allele Identifier: CA1879990345

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820230_127820231delinsAC , CM000671.2:g.127820230_127820231delinsAC	GRCh38
NC_000009.11:g.130582509_130582510delinsAC , CM000671.1:g.130582509_130582510delinsAC	GRCh37
NC_000009.10:g.129622330_129622331delinsAC	NCBI36
NG_009551.1:g.39538_39539delinsGT , LRG_589:g.39538_39539delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-194_589-193delinsGT	ENSP00000479015.1:n.589-194_589-193delinsGT
ENST00000373203.9:c.1135-194_1135-193delinsGT MANE Select	ENSP00000362299.4:n.1135-194_1135-193delinsGT
ENST00000344849.4:c.1135-194_1135-193delinsGT	ENSP00000341917.3:n.1135-194_1135-193delinsGT
ENST00000373203.8:c.1135-194_1135-193delinsGT	ENSP00000362299.4:n.1135-194_1135-193delinsGT
ENST00000480266.5:c.589-194_589-193delinsGT	ENSP00000479015.1:n.589-194_589-193delinsGT
ENST00000486329.1:n.103-194_103-193delinsGT
NM_000118.3:c.1135-194_1135-193delinsGT , LRG_589t1:c.1135-194_1135-193delinsGT	NP_000109.1:n.1135-194_1135-193delinsGT
NM_001114753.2:c.1135-194_1135-193delinsGT , LRG_589t2:c.1135-194_1135-193delinsGT	NP_001108225.1:n.1135-194_1135-193delinsGT
NM_001278138.1:c.589-194_589-193delinsGT	NP_001265067.1:n.589-194_589-193delinsGT
NR_136302.1:n.1569-965_1569-964delinsAC
NM_001114753.3:c.1135-194_1135-193delinsGT MANE Select	NP_001108225.1:n.1135-194_1135-193delinsGT
NM_001278138.2:c.589-194_589-193delinsGT	NP_001265067.1:n.589-194_589-193delinsGT