Canonical Allele Identifier: CA1879998650

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854288_127854289delinsCT , CM000671.2:g.127854288_127854289delinsCT	GRCh38
NC_000009.11:g.130616567_130616568delinsCT , CM000671.1:g.130616567_130616568delinsCT	GRCh37
NC_000009.10:g.129656388_129656389delinsCT	NCBI36
NG_009551.1:g.5480_5481delinsAG , LRG_589:g.5480_5481delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.67_67+1delinsAG
ENST00000344849.4:c.67_67+1delinsAG
ENST00000373203.8:c.67_67+1delinsAG
NM_000118.3:c.67_67+1delinsAG , LRG_589t1:c.67_67+1delinsAG
NM_001114753.2:c.67_67+1delinsAG , LRG_589t2:c.67_67+1delinsAG
NM_001114753.3:c.67_67+1delinsAG