Canonical Allele Identifier: CA653711641

Gene: ENG

Linked Data

• COSMIC: COSN19170330

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815123_127815124insG , CM000671.2:g.127815123_127815124insG	GRCh38
NC_000009.11:g.130577402_130577403insG , CM000671.1:g.130577402_130577403insG	GRCh37
NC_000009.10:g.129617223_129617224insG	NCBI36
NG_009551.1:g.44645_44646insC , LRG_589:g.44645_44646insC
NG_023245.1:g.17249_17250insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*558_*559insC	ENSP00000479015.1:n.*558_*559insC
ENST00000373203.9:c.*558_*559insC MANE Select	ENSP00000362299.4:n.*558_*559insC
ENST00000344849.4:c.*793_*794insC	ENSP00000341917.3:n.*793_*794insC
ENST00000373203.8:c.*558_*559insC	ENSP00000362299.4:n.*558_*559insC
ENST00000480266.5:c.*558_*559insC	ENSP00000479015.1:n.*558_*559insC
NM_000118.3:c.*793_*794insC , LRG_589t1:c.*793_*794insC	NP_000109.1:n.*793_*794insC
NM_001114753.2:c.*558_*559insC , LRG_589t2:c.*558_*559insC	NP_001108225.1:n.*558_*559insC
NM_001278138.1:c.*558_*559insC	NP_001265067.1:n.*558_*559insC
NM_001114753.3:c.*558_*559insC MANE Select	NP_001108225.1:n.*558_*559insC
NM_001278138.2:c.*558_*559insC	NP_001265067.1:n.*558_*559insC