Canonical Allele Identifier: CA1879988709

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819521_127819522delinsCA , CM000671.2:g.127819521_127819522delinsCA	GRCh38
NC_000009.11:g.130581800_130581801delinsCA , CM000671.1:g.130581800_130581801delinsCA	GRCh37
NC_000009.10:g.129621621_129621622delinsCA	NCBI36
NG_009551.1:g.40247_40248delinsTG , LRG_589:g.40247_40248delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.765+100_765+101delinsTG	ENSP00000479015.1:n.765+100_765+101delinsTG
ENST00000373203.9:c.1311+100_1311+101delinsTG MANE Select	ENSP00000362299.4:n.1311+100_1311+101delinsTG
ENST00000344849.4:c.1311+100_1311+101delinsTG	ENSP00000341917.3:n.1311+100_1311+101delinsTG
ENST00000373203.8:c.1311+100_1311+101delinsTG	ENSP00000362299.4:n.1311+100_1311+101delinsTG
ENST00000480266.5:c.765+100_765+101delinsTG	ENSP00000479015.1:n.765+100_765+101delinsTG
ENST00000486329.1:n.379_380delinsTG
NM_000118.3:c.1311+100_1311+101delinsTG , LRG_589t1:c.1311+100_1311+101delinsTG	NP_000109.1:n.1311+100_1311+101delinsTG
NM_001114753.2:c.1311+100_1311+101delinsTG , LRG_589t2:c.1311+100_1311+101delinsTG	NP_001108225.1:n.1311+100_1311+101delinsTG
NM_001278138.1:c.765+100_765+101delinsTG	NP_001265067.1:n.765+100_765+101delinsTG
NR_136302.1:n.1568+810_1568+811delinsCA
NM_001114753.3:c.1311+100_1311+101delinsTG MANE Select	NP_001108225.1:n.1311+100_1311+101delinsTG
NM_001278138.2:c.765+100_765+101delinsTG	NP_001265067.1:n.765+100_765+101delinsTG