Canonical Allele Identifier: CA1879981812

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829725_127829726delinsGC , CM000671.2:g.127829725_127829726delinsGC	GRCh38
NC_000009.11:g.130592004_130592005delinsGC , CM000671.1:g.130592004_130592005delinsGC	GRCh37
NC_000009.10:g.129631825_129631826delinsGC	NCBI36
NG_009551.1:g.30043_30044delinsGC , LRG_589:g.30043_30044delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-226_-225delinsGC	ENSP00000479015.1:n.-226_-225delinsGC
ENST00000373203.9:c.321_322delinsGC MANE Select	ENSP00000362299.4:p.Leu107=
ENST00000344849.4:c.321_322delinsGC	ENSP00000341917.3:p.Leu107=
ENST00000373203.8:c.321_322delinsGC	ENSP00000362299.4:p.Leu107=
ENST00000462196.1:n.79_80delinsGC
ENST00000480266.5:c.-226_-225delinsGC	ENSP00000479015.1:n.-226_-225delinsGC
NM_000118.3:c.321_322delinsGC , LRG_589t1:c.321_322delinsGC	NP_000109.1:p.Leu107=
NM_001114753.2:c.321_322delinsGC , LRG_589t2:c.321_322delinsGC	NP_001108225.1:p.Leu107=
NM_001278138.1:c.-226_-225delinsGC	NP_001265067.1:n.-226_-225delinsGC
XR_001746952.2:n.83-2673_83-2672delinsGC
NM_001114753.3:c.321_322delinsGC MANE Select	NP_001108225.1:p.Leu107=
NM_001278138.2:c.-226_-225delinsGC	NP_001265067.1:n.-226_-225delinsGC