Canonical Allele Identifier: CA2695211279

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819968del , CM000671.2:g.127819968del	GRCh38
NC_000009.11:g.130582247del , CM000671.1:g.130582247del	GRCh37
NC_000009.10:g.129622068del	NCBI36
NG_009551.1:g.39802del , LRG_589:g.39802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.659del	ENSP00000479015.1:p.Lys220SerfsTer19
ENST00000373203.9:c.1205del MANE Select	ENSP00000362299.4:p.Lys402SerfsTer19
ENST00000344849.4:c.1205del	ENSP00000341917.3:p.Lys402SerfsTer19
ENST00000373203.8:c.1205del	ENSP00000362299.4:p.Lys402SerfsTer19
ENST00000480266.5:c.659del	ENSP00000479015.1:p.Lys220SerfsTer19
ENST00000486329.1:n.173del
NM_000118.3:c.1205del , LRG_589t1:c.1205del	NP_000109.1:p.Lys402SerfsTer19
NM_001114753.2:c.1205del , LRG_589t2:c.1205del	NP_001108225.1:p.Lys402SerfsTer19
NM_001278138.1:c.659del	NP_001265067.1:p.Lys220SerfsTer19
NR_136302.1:n.1569-1227del
NM_001114753.3:c.1205del MANE Select	NP_001108225.1:p.Lys402SerfsTer19
NM_001278138.2:c.659del	NP_001265067.1:p.Lys220SerfsTer19