Canonical Allele Identifier: CA13910317

Gene: DLEU1

Linked Data

• dbSNP Id: rs201789
• gnomAD v2: 13-50986118-T-C
• gnomAD v3: 13-50411982-T-C
• gnomAD v4: 13-50411982-T-C
• MyVariant Identifiers: chr13:g.50986118T>C (hg19) ; chr13:g.50411982T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50411982T>C , CM000675.2:g.50411982T>C	GRCh38
NC_000013.10:g.50986118T>C , CM000675.1:g.50986118T>C	GRCh37
NC_000013.9:g.49884119T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000461527.6:n.556-3108T>C
ENST00000463474.6:n.600-21431T>C
ENST00000467721.5:n.535-3107T>C
ENST00000468168.5:n.535-21431T>C
ENST00000468522.5:n.441-3107T>C
ENST00000469095.5:n.820-3107T>C
ENST00000469127.5:n.207-3107T>C
ENST00000470726.6:n.95-3107T>C
ENST00000474630.5:n.95-3107T>C
ENST00000475913.5:n.286-21431T>C
ENST00000476738.5:n.388-3107T>C
ENST00000479420.5:n.95-3107T>C
ENST00000480262.2:n.454-3108T>C
ENST00000484869.6:n.745-995T>C
ENST00000485007.5:n.286-3107T>C
ENST00000490577.5:n.1638-21431T>C
ENST00000491341.5:n.535-3107T>C
ENST00000491482.5:n.95-21431T>C
ENST00000491615.5:n.535-3107T>C
NR_109974.1:n.537-21431T>C