Canonical Allele Identifier: CA2554754291

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824526_127824527insC , CM000671.2:g.127824526_127824527insC	GRCh38
NC_000009.11:g.130586805_130586806insC , CM000671.1:g.130586805_130586806insC	GRCh37
NC_000009.10:g.129626626_129626627insC	NCBI36
NG_009551.1:g.35242_35243insG , LRG_589:g.35242_35243insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-81_446-80insG	ENSP00000479015.1:n.446-81_446-80insG
ENST00000373203.9:c.992-81_992-80insG MANE Select	ENSP00000362299.4:n.992-81_992-80insG
ENST00000344849.4:c.992-81_992-80insG	ENSP00000341917.3:n.992-81_992-80insG
ENST00000373203.8:c.992-81_992-80insG	ENSP00000362299.4:n.992-81_992-80insG
ENST00000480266.5:c.446-81_446-80insG	ENSP00000479015.1:n.446-81_446-80insG
NM_000118.3:c.992-81_992-80insG , LRG_589t1:c.992-81_992-80insG	NP_000109.1:n.992-81_992-80insG
NM_001114753.2:c.992-81_992-80insG , LRG_589t2:c.992-81_992-80insG	NP_001108225.1:n.992-81_992-80insG
NM_001278138.1:c.446-81_446-80insG	NP_001265067.1:n.446-81_446-80insG
NM_001114753.3:c.992-81_992-80insG MANE Select	NP_001108225.1:n.992-81_992-80insG
NM_001278138.2:c.446-81_446-80insG	NP_001265067.1:n.446-81_446-80insG