Canonical Allele Identifier: CA1879973661

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824895_127824896delinsAG , CM000671.2:g.127824895_127824896delinsAG	GRCh38
NC_000009.11:g.130587174_130587175delinsAG , CM000671.1:g.130587174_130587175delinsAG	GRCh37
NC_000009.10:g.129626995_129626996delinsAG	NCBI36
NG_009551.1:g.34873_34874delinsCT , LRG_589:g.34873_34874delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.349_350delinsCT	ENSP00000479015.1:p.Leu117=
ENST00000373203.9:c.895_896delinsCT MANE Select	ENSP00000362299.4:p.Leu299=
ENST00000344849.4:c.895_896delinsCT	ENSP00000341917.3:p.Leu299=
ENST00000373203.8:c.895_896delinsCT	ENSP00000362299.4:p.Leu299=
ENST00000480266.5:c.349_350delinsCT	ENSP00000479015.1:p.Leu117=
NM_000118.3:c.895_896delinsCT , LRG_589t1:c.895_896delinsCT	NP_000109.1:p.Leu299=
NM_001114753.2:c.895_896delinsCT , LRG_589t2:c.895_896delinsCT	NP_001108225.1:p.Leu299=
NM_001278138.1:c.349_350delinsCT	NP_001265067.1:p.Leu117=
NM_001114753.3:c.895_896delinsCT MANE Select	NP_001108225.1:p.Leu299=
NM_001278138.2:c.349_350delinsCT	NP_001265067.1:p.Leu117=