Canonical Allele Identifier: CA2091056852
Gene: DLEU7 HGNC NCBI
DLEU7-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1876740328

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50816490A>G , CM000675.2:g.50816490A>G GRCh38
NC_000013.10:g.51390626A>G , CM000675.1:g.51390626A>G GRCh37
NC_000013.9:g.50288627A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651265.1:n.569+6703T>C (DLEU7)
ENST00000651397.1:n.426+26698T>C (DLEU7)
ENST00000400393.3:c.459+26698T>C (DLEU7) ENSP00000420976.1:n.459+26698T>C
NM_198989.2:c.459+26698T>C (DLEU7) NP_945340.2:n.459+26698T>C
NM_198989.3:c.459+26698T>C (DLEU7) NP_945340.2:n.459+26698T>C
NR_046551.1:n.300-2031A>G (DLEU7-AS1)
XM_011534973.1:c.459+26698T>C (DLEU7) XP_011533275.1:n.459+26698T>C