Canonical Allele Identifier: CA609912179
Gene: DLEU7 HGNC NCBI
DLEU7-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1255112234
gnomAD v2: 13-51390648-A-G
gnomAD v3: 13-50816512-A-G
gnomAD v4: 13-50816512-A-G
MyVariant Identifiers: chr13:g.51390648A>G (hg19) chr13:g.50816512A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50816512A>G , CM000675.2:g.50816512A>G GRCh38
NC_000013.10:g.51390648A>G , CM000675.1:g.51390648A>G GRCh37
NC_000013.9:g.50288649A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651265.1:n.569+6681T>C (DLEU7)
ENST00000651397.1:n.426+26676T>C (DLEU7)
ENST00000400393.3:c.459+26676T>C (DLEU7) ENSP00000420976.1:n.459+26676T>C
NM_198989.2:c.459+26676T>C (DLEU7) NP_945340.2:n.459+26676T>C
NM_198989.3:c.459+26676T>C (DLEU7) NP_945340.2:n.459+26676T>C
NR_046551.1:n.300-2009A>G (DLEU7-AS1)
XM_011534973.1:c.459+26676T>C (DLEU7) XP_011533275.1:n.459+26676T>C
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