Canonical Allele Identifier: CA2090971392

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620190_50620195delinsCTACTT , CM000675.2:g.50620190_50620195delinsCTACTT GRCh38
NC_000013.10:g.51194326_51194331delinsCTACTT , CM000675.1:g.51194326_51194331delinsCTACTT GRCh37
NC_000013.9:g.50092327_50092332delinsCTACTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63711_1033+63716delinsAAGTAG (DLEU7)
ENST00000470726.6:n.347-99457_347-99452delinsCTACTT (DLEU1)
ENST00000479420.5:n.560-28400_560-28395delinsCTACTT (DLEU1)
ENST00000484869.6:n.1330-11087_1330-11082delinsCTACTT (DLEU1)