Canonical Allele Identifier: CA698828794

Linked Data

dbSNP Id: rs1370517784

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620312_50620317del , CM000675.2:g.50620312_50620317del GRCh38
NC_000013.10:g.51194448_51194453del , CM000675.1:g.51194448_51194453del GRCh37
NC_000013.9:g.50092449_50092454del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63593_1033+63598del (DLEU7)
ENST00000470726.6:n.347-99335_347-99330del (DLEU1)
ENST00000479420.5:n.560-28278_560-28273del (DLEU1)
ENST00000484869.6:n.1330-10965_1330-10960del (DLEU1)