Canonical Allele Identifier: CA609912170
Gene: DLEU7 HGNC NCBI
DLEU7-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1305179622
gnomAD v2: 13-51390569-T-TA
gnomAD v3: 13-50816433-T-TA
gnomAD v4: 13-50816433-T-TA
MyVariant Identifiers: chr13:g.51390569_51390570insA (hg19) chr13:g.50816433_50816434insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50816439dup , CM000675.2:g.50816439dup GRCh38
NC_000013.10:g.51390575dup , CM000675.1:g.51390575dup GRCh37
NC_000013.9:g.50288576dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651265.1:n.569+6759dup (DLEU7)
ENST00000651397.1:n.426+26754dup (DLEU7)
ENST00000400393.3:c.459+26754dup (DLEU7) ENSP00000420976.1:n.459+26754dup
NM_198989.2:c.459+26754dup (DLEU7) NP_945340.2:n.459+26754dup
NM_198989.3:c.459+26754dup (DLEU7) NP_945340.2:n.459+26754dup
NR_046551.1:n.300-2082dup (DLEU7-AS1)
XM_011534973.1:c.459+26754dup (DLEU7) XP_011533275.1:n.459+26754dup
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