Canonical Allele Identifier: CA1879977358

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826536_127826537delinsTG , CM000671.2:g.127826536_127826537delinsTG	GRCh38
NC_000009.11:g.130588815_130588816delinsTG , CM000671.1:g.130588815_130588816delinsTG	GRCh37
NC_000009.10:g.129628636_129628637delinsTG	NCBI36
NG_009551.1:g.33232_33233delinsCA , LRG_589:g.33232_33233delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-51_-50delinsCA	ENSP00000479015.1:n.-51_-50delinsCA
ENST00000373203.9:c.496_497delinsCA MANE Select	ENSP00000362299.4:p.Gln166=
ENST00000344849.4:c.496_497delinsCA	ENSP00000341917.3:p.Gln166=
ENST00000373203.8:c.496_497delinsCA	ENSP00000362299.4:p.Gln166=
ENST00000462196.1:n.396_397delinsCA
ENST00000480266.5:c.-51_-50delinsCA	ENSP00000479015.1:n.-51_-50delinsCA
NM_000118.3:c.496_497delinsCA , LRG_589t1:c.496_497delinsCA	NP_000109.1:p.Gln166=
NM_001114753.2:c.496_497delinsCA , LRG_589t2:c.496_497delinsCA	NP_001108225.1:p.Gln166=
NM_001278138.1:c.-51_-50delinsCA	NP_001265067.1:n.-51_-50delinsCA
XR_001746952.2:n.82+1078_82+1079delinsTG
NM_001114753.3:c.496_497delinsCA MANE Select	NP_001108225.1:p.Gln166=
NM_001278138.2:c.-51_-50delinsCA	NP_001265067.1:n.-51_-50delinsCA