Canonical Allele Identifier: CA2691808679

Gene: ENG

Linked Data

• gnomAD v4: 9-127818390-G-GGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127818390_127818391insGCA , CM000671.2:g.127818390_127818391insGCA	GRCh38
NC_000009.11:g.130580669_130580670insGCA , CM000671.1:g.130580669_130580670insGCA	GRCh37
NC_000009.10:g.129620490_129620491insGCA	NCBI36
NG_009551.1:g.41378_41379insTGC , LRG_589:g.41378_41379insTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.883-14_883-13insTGC	ENSP00000479015.1:n.883-14_883-13insTGC
ENST00000373203.9:c.1429-14_1429-13insTGC MANE Select	ENSP00000362299.4:n.1429-14_1429-13insTGC
ENST00000344849.4:c.1429-14_1429-13insTGC	ENSP00000341917.3:n.1429-14_1429-13insTGC
ENST00000373203.8:c.1429-14_1429-13insTGC	ENSP00000362299.4:n.1429-14_1429-13insTGC
ENST00000480266.5:c.883-14_883-13insTGC	ENSP00000479015.1:n.883-14_883-13insTGC
NM_000118.3:c.1429-14_1429-13insTGC , LRG_589t1:c.1429-14_1429-13insTGC	NP_000109.1:n.1429-14_1429-13insTGC
NM_001114753.2:c.1429-14_1429-13insTGC , LRG_589t2:c.1429-14_1429-13insTGC	NP_001108225.1:n.1429-14_1429-13insTGC
NM_001278138.1:c.883-14_883-13insTGC	NP_001265067.1:n.883-14_883-13insTGC
NR_136302.1:n.1456+1_1456+2insGCA
NM_001114753.3:c.1429-14_1429-13insTGC MANE Select	NP_001108225.1:n.1429-14_1429-13insTGC
NM_001278138.2:c.883-14_883-13insTGC	NP_001265067.1:n.883-14_883-13insTGC