Canonical Allele Identifier: CA2691807906

Gene: ENG

Linked Data

• gnomAD v4: 9-127824511-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824511_127824512insAT , CM000671.2:g.127824511_127824512insAT	GRCh38
NC_000009.11:g.130586790_130586791insAT , CM000671.1:g.130586790_130586791insAT	GRCh37
NC_000009.10:g.129626611_129626612insAT	NCBI36
NG_009551.1:g.35257_35258insAT , LRG_589:g.35257_35258insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-66_446-65insAT	ENSP00000479015.1:n.446-66_446-65insAT
ENST00000373203.9:c.992-66_992-65insAT MANE Select	ENSP00000362299.4:n.992-66_992-65insAT
ENST00000344849.4:c.992-66_992-65insAT	ENSP00000341917.3:n.992-66_992-65insAT
ENST00000373203.8:c.992-66_992-65insAT	ENSP00000362299.4:n.992-66_992-65insAT
ENST00000480266.5:c.446-66_446-65insAT	ENSP00000479015.1:n.446-66_446-65insAT
NM_000118.3:c.992-66_992-65insAT , LRG_589t1:c.992-66_992-65insAT	NP_000109.1:n.992-66_992-65insAT
NM_001114753.2:c.992-66_992-65insAT , LRG_589t2:c.992-66_992-65insAT	NP_001108225.1:n.992-66_992-65insAT
NM_001278138.1:c.446-66_446-65insAT	NP_001265067.1:n.446-66_446-65insAT
NM_001114753.3:c.992-66_992-65insAT MANE Select	NP_001108225.1:n.992-66_992-65insAT
NM_001278138.2:c.446-66_446-65insAT	NP_001265067.1:n.446-66_446-65insAT