Canonical Allele Identifier: CA2831039755
Gene: BTD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15635434del , CM000665.2:g.15635434del GRCh38
NC_000003.11:g.15676941del , CM000665.1:g.15676941del GRCh37
NC_000003.10:g.15651945del NCBI36
NG_008019.1:g.38687del
NG_008019.2:g.39083del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436193.6:c.-6del ENSP00000394277.2:n.-6del
ENST00000671928.2:c.-6del ENSP00000500069.2:n.-6del
ENST00000672892.2:c.-6del ENSP00000499944.2:n.-6del
ENST00000303498.10:c.-6del ENSP00000306477.6:n.-6del
ENST00000417015.3:c.-6del ENSP00000403775.3:n.-6del
ENST00000427382.2:c.-6del ENSP00000397113.2:n.-6del
ENST00000437172.6:c.-6del ENSP00000400995.2:n.-6del
ENST00000449107.7:c.-6del ENSP00000388212.2:n.-6del
ENST00000467027.6:n.834del
ENST00000482824.2:c.-6del ENSP00000494864.1:n.-6del
ENST00000643237.3:c.-6del MANE Select ENSP00000495254.2:n.-6del
ENST00000646371.1:c.-6del ENSP00000495866.1:n.-6del
ENST00000672065.1:c.55del ENSP00000500403.1:p.Cys19AlafsTer?
ENST00000672112.1:c.61del ENSP00000500193.1:p.Cys21AlafsTer?
ENST00000672141.1:c.-6del ENSP00000500210.1:n.-6del
ENST00000672336.1:c.-6del ENSP00000500267.1:n.-6del
ENST00000672427.1:c.-6del ENSP00000500131.1:n.-6del
ENST00000672760.1:c.-6del ENSP00000500530.1:n.-6del
ENST00000673467.1:c.-6del ENSP00000500288.1:n.-6del
ENST00000673620.1:c.-6del ENSP00000500325.1:n.-6del
ENST00000303498.9:c.55del ENSP00000306477.5:p.Cys19AlafsTer?
ENST00000383778.5:c.-6del ENSP00000373288.4:n.-6del
ENST00000417015.1:c.*306del ENSP00000403775.1:n.*306del
ENST00000427382.1:c.-6del ENSP00000397113.1:n.-6del
ENST00000436193.5:c.-6del ENSP00000394277.1:n.-6del
ENST00000437172.5:c.61del ENSP00000400995.1:p.Cys21AlafsTer?
ENST00000449107.5:c.61del ENSP00000388212.1:p.Cys21AlafsTer?
ENST00000467027.5:n.381del
ENST00000482824.1:n.130del
ENST00000494021.1:n.412del
NM_000060.3:c.55del NP_000051.1:p.Cys19AlafsTer?
NM_001281723.1:c.61del NP_001268652.1:p.Cys21AlafsTer?
NM_001281724.1:c.61del NP_001268653.1:p.Cys21AlafsTer?
NM_001281725.1:c.-6del NP_001268654.1:n.-6del
NM_001281726.1:c.55del NP_001268655.1:p.Cys19AlafsTer?
XM_006713314.2:c.-6del XP_006713377.1:n.-6del
XM_011534041.1:c.-6del XP_011532343.1:n.-6del
NM_000060.4:c.55del NP_000051.1:p.Cys19AlafsTer?
NM_001281723.2:c.61del NP_001268652.1:p.Cys21AlafsTer?
NM_001281724.2:c.61del NP_001268653.1:p.Cys21AlafsTer?
NM_001281725.2:c.-6del NP_001268654.1:n.-6del
NM_001323582.1:c.-6del NP_001310511.1:n.-6del
XM_011534041.2:c.-6del XP_011532343.1:n.-6del
XM_017007088.1:c.-6del XP_016862577.1:n.-6del
XM_024453724.1:c.-6del XP_024309492.1:n.-6del
NM_001281723.3:c.-6del NP_001268652.2:n.-6del
NM_001281724.3:c.-6del NP_001268653.2:n.-6del
NM_001370658.1:c.-6del MANE Select NP_001357587.1:n.-6del
NM_001370752.1:c.-6del NP_001357681.1:n.-6del
NM_001370753.1:c.-6del NP_001357682.1:n.-6del
NM_001281726.2:c.-6del NP_001268655.2:n.-6del