Canonical Allele Identifier: CA249927782

Gene: DLEU1

Linked Data

• dbSNP Id: rs906178809
• gnomAD v3: 13-50268342-CAA-C
• gnomAD v4: 13-50268342-CAA-C
• MyVariant Identifiers: chr13:g.50842479_50842480del (hg19) ; chr13:g.50268343_50268344del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50268344_50268345del , CM000675.2:g.50268344_50268345del	GRCh38
NC_000013.10:g.50842480_50842481del , CM000675.1:g.50842480_50842481del	GRCh37
NC_000013.9:g.49740481_49740482del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461527.6:n.441-6588_441-6587del
ENST00000463474.6:n.441-70332_441-70331del
ENST00000467721.5:n.441-121854_441-121853del
ENST00000468168.5:n.441-121854_441-121853del
ENST00000468522.5:n.441-146745_441-146744del
ENST00000473075.2:n.105+19966_105+19967del
ENST00000475913.5:n.191+82274_191+82275del
ENST00000476738.5:n.388-146745_388-146744del
ENST00000483444.5:n.97+43967_97+43968del
ENST00000484529.5:n.192-6588_192-6587del
ENST00000485007.5:n.191+82274_191+82275del
ENST00000486895.5:n.388-121854_388-121853del
ENST00000490577.5:n.1637+110268_1637+110269del
ENST00000491341.5:n.441-121854_441-121853del
ENST00000491615.5:n.441-121854_441-121853del
NR_109974.1:n.443-121854_443-121853del