Canonical Allele Identifier: CA2018023352
Community Standard Title: NC_000013.11:g.50492487C=
Gene: DLEU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50492487C= , CM000675.2:g.50492487C= GRCh38
NC_000013.10:g.51066623C= , CM000675.1:g.51066623C= GRCh37
NC_000013.9:g.49964624C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109974.1:n.675-164C=
ENST00000460525.5:n.253-164C=
ENST00000461527.6:n.807-164C=
ENST00000462427.1:n.253-35379C=
ENST00000463474.6:n.849+34374C=
ENST00000467721.5:n.787-35379C=
ENST00000468168.5:n.673-164C=
ENST00000468522.5:n.693-164C=
ENST00000469095.5:n.1072-164C=
ENST00000470593.5:n.115-35379C=
ENST00000470726.6:n.346+58937C=
ENST00000472136.5:n.253-164C=
ENST00000474630.5:n.209-164C=
ENST00000475913.5:n.424-164C=
ENST00000476738.5:n.640-35379C=
ENST00000479420.5:n.347-164C=
ENST00000484869.6:n.1150-164C=
ENST00000485007.5:n.538-35379C=
ENST00000490577.5:n.1776-164C=
ENST00000491341.5:n.787-35693C=
ENST00000491482.5:n.233-35379C=
ENST00000491615.5:n.787-164C=