Canonical Allele Identifier: CA1879972384

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824294_127824295delinsGT , CM000671.2:g.127824294_127824295delinsGT	GRCh38
NC_000009.11:g.130586573_130586574delinsGT , CM000671.1:g.130586573_130586574delinsGT	GRCh37
NC_000009.10:g.129626394_129626395delinsGT	NCBI36
NG_009551.1:g.35474_35475delinsAC , LRG_589:g.35474_35475delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.588+9_588+10delinsAC	ENSP00000479015.1:n.588+9_588+10delinsAC
ENST00000373203.9:c.1134+9_1134+10delinsAC MANE Select	ENSP00000362299.4:n.1134+9_1134+10delinsA...
ENST00000344849.4:c.1134+9_1134+10delinsAC	ENSP00000341917.3:n.1134+9_1134+10delinsA...
ENST00000373203.8:c.1134+9_1134+10delinsAC	ENSP00000362299.4:n.1134+9_1134+10delinsA...
ENST00000480266.5:c.588+9_588+10delinsAC	ENSP00000479015.1:n.588+9_588+10delinsAC
ENST00000486329.1:n.102+9_102+10delinsAC
NM_000118.3:c.1134+9_1134+10delinsAC , LRG_589t1:c.1134+9_1134+10delinsAC	NP_000109.1:n.1134+9_1134+10delinsAC
NM_001114753.2:c.1134+9_1134+10delinsAC , LRG_589t2:c.1134+9_1134+10delinsAC	NP_001108225.1:n.1134+9_1134+10delinsAC
NM_001278138.1:c.588+9_588+10delinsAC	NP_001265067.1:n.588+9_588+10delinsAC
NM_001114753.3:c.1134+9_1134+10delinsAC MANE Select	NP_001108225.1:n.1134+9_1134+10delinsAC
NM_001278138.2:c.588+9_588+10delinsAC	NP_001265067.1:n.588+9_588+10delinsAC