Canonical Allele Identifier: CA220319
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 92399
ClinVar RCV Id: RCV000178031 RCV000790753
dbSNP Id: rs398123138
MyVariant Identifiers: chr3:g.15686871_15686875del (hg19) chr3:g.15686871_15686875delGGATG (hg19) chr3:g.15645364_15645368del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15645364_15645368del , CM000665.2:g.15645364_15645368del GRCh38
NC_000003.11:g.15686871_15686875del , CM000665.1:g.15686871_15686875del GRCh37
NC_000003.10:g.15661875_15661879del NCBI36
NG_008019.1:g.48617_48621del
NG_008019.2:g.49013_49017del

Transcript Alleles

HGVS Amino-acid change
ENST00000436193.6:c.1448_1452del ENSP00000394277.2:p.Gly483AspfsTer6
ENST00000671928.2:c.399+3307_399+3311del ENSP00000500069.2:n.399+3307_399+3311del
ENST00000672892.2:c.1015+433_1015+437del ENSP00000499944.2:n.1015+433_1015+437del
ENST00000303498.10:c.1448_1452del ENSP00000306477.6:p.Gly483AspfsTer6
ENST00000427382.2:c.1448_1452del ENSP00000397113.2:p.Gly483AspfsTer6
ENST00000437172.6:c.1448_1452del ENSP00000400995.2:p.Gly483AspfsTer6
ENST00000449107.7:c.1448_1452del ENSP00000388212.2:p.Gly483AspfsTer6
ENST00000643237.3:c.1448_1452del MANE Select ENSP00000495254.2:p.Gly483AspfsTer6
ENST00000646371.1:c.1448_1452del ENSP00000495866.1:p.Gly483AspfsTer6
ENST00000671928.1:c.165+3307_165+3311del ENSP00000500069.1:n.165+3307_165+3311del
ENST00000672065.1:c.1508_1512del ENSP00000500403.1:p.Gly503AspfsTer6
ENST00000672112.1:c.1514_1518del ENSP00000500193.1:p.Gly505AspfsTer6
ENST00000672141.1:c.399+3307_399+3311del ENSP00000500210.1:n.399+3307_399+3311del
ENST00000672427.1:c.1015+433_1015+437del ENSP00000500131.1:n.1015+433_1015+437del
ENST00000672760.1:c.399+3307_399+3311del ENSP00000500530.1:n.399+3307_399+3311del
ENST00000672892.1:c.793+433_793+437del ENSP00000499944.1:n.793+433_793+437del
ENST00000673467.1:c.399+3307_399+3311del ENSP00000500288.1:n.399+3307_399+3311del
ENST00000673620.1:c.399+3307_399+3311del ENSP00000500325.1:n.399+3307_399+3311del
ENST00000303498.9:c.1508_1512del ENSP00000306477.5:p.Gly503AspfsTer6
ENST00000383778.5:c.1448_1452del ENSP00000373288.4:p.Gly483AspfsTer6
ENST00000437172.5:c.1514_1518del ENSP00000400995.1:p.Gly505AspfsTer6
ENST00000449107.5:c.1514_1518del ENSP00000388212.1:p.Gly505AspfsTer6
NM_000060.3:c.1508_1512del NP_000051.1:p.Gly503AspfsTer6
NM_001281723.1:c.1514_1518del NP_001268652.1:p.Gly505AspfsTer6
NM_001281724.1:c.1514_1518del NP_001268653.1:p.Gly505AspfsTer6
NM_001281725.1:c.1448_1452del NP_001268654.1:p.Gly483AspfsTer6
XM_006713314.2:c.1448_1452del XP_006713377.1:p.Gly483AspfsTer6
XM_011534041.1:c.1448_1452del XP_011532343.1:p.Gly483AspfsTer6
NM_000060.4:c.1508_1512del NP_000051.1:p.Gly503AspfsTer6
NM_001281723.2:c.1514_1518del NP_001268652.1:p.Gly505AspfsTer6
NM_001281724.2:c.1514_1518del NP_001268653.1:p.Gly505AspfsTer6
NM_001281725.2:c.1448_1452del NP_001268654.1:p.Gly483AspfsTer6
NM_001323582.1:c.1448_1452del NP_001310511.1:p.Gly483AspfsTer6
XM_011534041.2:c.1448_1452del XP_011532343.1:p.Gly483AspfsTer6
XM_017007088.1:c.1448_1452del XP_016862577.1:p.Gly483AspfsTer6
XM_024453724.1:c.1448_1452del XP_024309492.1:p.Gly483AspfsTer6
NM_001281723.3:c.1448_1452del NP_001268652.2:p.Gly483AspfsTer6
NM_001281724.3:c.1448_1452del NP_001268653.2:p.Gly483AspfsTer6
NM_001370658.1:c.1448_1452del MANE Select NP_001357587.1:p.Gly483AspfsTer6
NM_001370752.1:c.1015+433_1015+437del NP_001357681.1:n.1015+433_1015+437del
NM_001370753.1:c.399+3307_399+3311del NP_001357682.1:n.399+3307_399+3311del
NM_001281726.2:c.*3226_*3230del NP_001268655.2:n.*3226_*3230del
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