Canonical Allele Identifier: CA609896911

Gene: DLEU1

Linked Data

• dbSNP Id: rs1380624172
• gnomAD v2: 13-50986112-G-A
• gnomAD v3: 13-50411976-G-A
• gnomAD v4: 13-50411976-G-A
• MyVariant Identifiers: chr13:g.50986112G>A (hg19) ; chr13:g.50411976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50411976G>A , CM000675.2:g.50411976G>A	GRCh38
NC_000013.10:g.50986112G>A , CM000675.1:g.50986112G>A	GRCh37
NC_000013.9:g.49884113G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461527.6:n.556-3114G>A
ENST00000463474.6:n.600-21437G>A
ENST00000467721.5:n.535-3113G>A
ENST00000468168.5:n.535-21437G>A
ENST00000468522.5:n.441-3113G>A
ENST00000469095.5:n.820-3113G>A
ENST00000469127.5:n.207-3113G>A
ENST00000470726.6:n.95-3113G>A
ENST00000474630.5:n.95-3113G>A
ENST00000475913.5:n.286-21437G>A
ENST00000476738.5:n.388-3113G>A
ENST00000479420.5:n.95-3113G>A
ENST00000480262.2:n.454-3114G>A
ENST00000484869.6:n.745-1001G>A
ENST00000485007.5:n.286-3113G>A
ENST00000490577.5:n.1638-21437G>A
ENST00000491341.5:n.535-3113G>A
ENST00000491482.5:n.95-21437G>A
ENST00000491615.5:n.535-3113G>A
NR_109974.1:n.537-21437G>A