Canonical Allele Identifier: CA10603021
Community Standard Title: NM_001114753.3(ENG):c.1554_1555del (p.Leu519AlafsTer8)
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127818251_127818252del , CM000671.2:g.127818251_127818252del GRCh38
NC_000009.11:g.130580530_130580531del , CM000671.1:g.130580530_130580531del GRCh37
NC_000009.10:g.129620351_129620352del NCBI36
NG_009551.1:g.41517_41518del , LRG_589:g.41517_41518del

Transcript Alleles

HGVS Amino-acid Change
NM_001114753.3:c.1554_1555del MANE Select NP_001108225.1:p.Leu519AlafsTer8
ENST00000373203.9:c.1554_1555del MANE Select ENSP00000362299.4:p.Leu519AlafsTer8
NM_000118.3:c.1554_1555del , LRG_589t1:c.1554_1555del NP_000109.1:p.Leu519AlafsTer8
NM_001114753.2:c.1554_1555del , LRG_589t2:c.1554_1555del NP_001108225.1:p.Leu519AlafsTer8
NM_001278138.1:c.1008_1009del NP_001265067.1:p.Leu337AlafsTer8
NM_001278138.2:c.1008_1009del NP_001265067.1:p.Leu337AlafsTer8
NR_136302.1:n.1378-60_1378-59del
ENST00000344849.4:c.1554_1555del ENSP00000341917.3:p.Leu519AlafsTer8
ENST00000373203.8:c.1554_1555del ENSP00000362299.4:p.Leu519AlafsTer8
ENST00000480266.5:c.1008_1009del ENSP00000479015.1:p.Leu337AlafsTer8
ENST00000480266.6:c.1008_1009del ENSP00000479015.1:p.Leu337AlafsTer8