Canonical Allele Identifier: CA1347664455
Gene: BTD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15644785G= , CM000665.2:g.15644785G= GRCh38
NC_000003.11:g.15686292G= , CM000665.1:g.15686292G= GRCh37
NC_000003.10:g.15661296G= NCBI36
NG_008019.1:g.48038G=
NG_008019.2:g.48434G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000436193.6:c.869G= ENSP00000394277.2:p.Gly290=
ENST00000671928.2:c.399+2728G= ENSP00000500069.2:n.399+2728G=
ENST00000672892.2:c.869G= ENSP00000499944.2:p.Gly290=
ENST00000303498.10:c.869G= ENSP00000306477.6:p.Gly290=
ENST00000427382.2:c.869G= ENSP00000397113.2:p.Gly290=
ENST00000437172.6:c.869G= ENSP00000400995.2:p.Gly290=
ENST00000449107.7:c.869G= ENSP00000388212.2:p.Gly290=
ENST00000643237.3:c.869G= MANE Select ENSP00000495254.2:p.Gly290=
ENST00000646371.1:c.869G= ENSP00000495866.1:p.Gly290=
ENST00000671928.1:c.165+2728G= ENSP00000500069.1:n.165+2728G=
ENST00000672065.1:c.929G= ENSP00000500403.1:p.Gly310=
ENST00000672112.1:c.935G= ENSP00000500193.1:p.Gly312=
ENST00000672141.1:c.399+2728G= ENSP00000500210.1:n.399+2728G=
ENST00000672427.1:c.869G= ENSP00000500131.1:p.Gly290=
ENST00000672760.1:c.399+2728G= ENSP00000500530.1:n.399+2728G=
ENST00000672892.1:c.647G= ENSP00000499944.1:p.Gly216=
ENST00000673467.1:c.399+2728G= ENSP00000500288.1:n.399+2728G=
ENST00000673620.1:c.399+2728G= ENSP00000500325.1:n.399+2728G=
ENST00000303498.9:c.929G= ENSP00000306477.5:p.Gly310=
ENST00000383778.5:c.869G= ENSP00000373288.4:p.Gly290=
ENST00000437172.5:c.935G= ENSP00000400995.1:p.Gly312=
ENST00000449107.5:c.935G= ENSP00000388212.1:p.Gly312=
NM_000060.3:c.929G= NP_000051.1:p.Gly310=
NM_001281723.1:c.935G= NP_001268652.1:p.Gly312=
NM_001281724.1:c.935G= NP_001268653.1:p.Gly312=
NM_001281725.1:c.869G= NP_001268654.1:p.Gly290=
XM_006713314.2:c.869G= XP_006713377.1:p.Gly290=
XM_011534041.1:c.869G= XP_011532343.1:p.Gly290=
NM_000060.4:c.929G= NP_000051.1:p.Gly310=
NM_001281723.2:c.935G= NP_001268652.1:p.Gly312=
NM_001281724.2:c.935G= NP_001268653.1:p.Gly312=
NM_001281725.2:c.869G= NP_001268654.1:p.Gly290=
NM_001323582.1:c.869G= NP_001310511.1:p.Gly290=
XM_011534041.2:c.869G= XP_011532343.1:p.Gly290=
XM_017007088.1:c.869G= XP_016862577.1:p.Gly290=
XM_024453724.1:c.869G= XP_024309492.1:p.Gly290=
NM_001281723.3:c.869G= NP_001268652.2:p.Gly290=
NM_001281724.3:c.869G= NP_001268653.2:p.Gly290=
NM_001370658.1:c.869G= MANE Select NP_001357587.1:p.Gly290=
NM_001370752.1:c.869G= NP_001357681.1:p.Gly290=
NM_001370753.1:c.399+2728G= NP_001357682.1:n.399+2728G=
NM_001281726.2:c.*2647G= NP_001268655.2:n.*2647G=