Canonical Allele Identifier: CA2691808471

Gene: ENG

Linked Data

• gnomAD v4: 9-127829785-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829785_127829786insA , CM000671.2:g.127829785_127829786insA	GRCh38
NC_000009.11:g.130592064_130592065insA , CM000671.1:g.130592064_130592065insA	GRCh37
NC_000009.10:g.129631885_129631886insA	NCBI36
NG_009551.1:g.29983_29984insT , LRG_589:g.29983_29984insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-286_-285insT	ENSP00000479015.1:n.-286_-285insT
ENST00000373203.9:c.261_262insT MANE Select	ENSP00000362299.4:p.Asn88Ter
ENST00000344849.4:c.261_262insT	ENSP00000341917.3:p.Asn88Ter
ENST00000373203.8:c.261_262insT	ENSP00000362299.4:p.Asn88Ter
ENST00000462196.1:n.19_20insT
ENST00000480266.5:c.-286_-285insT	ENSP00000479015.1:n.-286_-285insT
NM_000118.3:c.261_262insT , LRG_589t1:c.261_262insT	NP_000109.1:p.Asn88Ter
NM_001114753.2:c.261_262insT , LRG_589t2:c.261_262insT	NP_001108225.1:p.Asn88Ter
NM_001278138.1:c.-286_-285insT	NP_001265067.1:n.-286_-285insT
XR_001746952.2:n.83-2613_83-2612insA
NM_001114753.3:c.261_262insT MANE Select	NP_001108225.1:p.Asn88Ter
NM_001278138.2:c.-286_-285insT	NP_001265067.1:n.-286_-285insT