Canonical Allele Identifier: CA1879972843

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824473_127824477delinsCGGCT , CM000671.2:g.127824473_127824477delinsCGGCT	GRCh38
NC_000009.11:g.130586752_130586756delinsCGGCT , CM000671.1:g.130586752_130586756delinsCGGCT	GRCh37
NC_000009.10:g.129626573_129626577delinsCGGCT	NCBI36
NG_009551.1:g.35292_35296delinsAGCCG , LRG_589:g.35292_35296delinsAGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-31_446-27delinsAGCCG	ENSP00000479015.1:n.446-31_446-27delinsAGCCG
ENST00000373203.9:c.992-31_992-27delinsAGCCG MANE Select	ENSP00000362299.4:n.992-31_992-27delinsAGCCG
ENST00000344849.4:c.992-31_992-27delinsAGCCG	ENSP00000341917.3:n.992-31_992-27delinsAGCCG
ENST00000373203.8:c.992-31_992-27delinsAGCCG	ENSP00000362299.4:n.992-31_992-27delinsAGCCG
ENST00000480266.5:c.446-31_446-27delinsAGCCG	ENSP00000479015.1:n.446-31_446-27delinsAGCCG
NM_000118.3:c.992-31_992-27delinsAGCCG , LRG_589t1:c.992-31_992-27delinsAGCCG	NP_000109.1:n.992-31_992-27delinsAGCCG
NM_001114753.2:c.992-31_992-27delinsAGCCG , LRG_589t2:c.992-31_992-27delinsAGCCG	NP_001108225.1:n.992-31_992-27delinsAGCCG
NM_001278138.1:c.446-31_446-27delinsAGCCG	NP_001265067.1:n.446-31_446-27delinsAGCCG
NM_001114753.3:c.992-31_992-27delinsAGCCG MANE Select	NP_001108225.1:n.992-31_992-27delinsAGCCG
NM_001278138.2:c.446-31_446-27delinsAGCCG	NP_001265067.1:n.446-31_446-27delinsAGCCG