Canonical Allele Identifier: CA278332
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25083
ClinVar RCV Id: RCV000022008
dbSNP Id: rs397514418
gnomAD v2: 3-15686702-C-T
gnomAD v4: 3-15645195-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15645195C>T , CM000665.2:g.15645195C>T GRCh38
NC_000003.11:g.15686702C>T , CM000665.1:g.15686702C>T GRCh37
NC_000003.10:g.15661706C>T NCBI36
NG_008019.1:g.48448C>T
NG_008019.2:g.48844C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000436193.6:c.1279C>T ENSP00000394277.2:p.His427Tyr
ENST00000671928.2:c.399+3138C>T ENSP00000500069.2:n.399+3138C>T
ENST00000672892.2:c.1015+264C>T ENSP00000499944.2:n.1015+264C>T
ENST00000303498.10:c.1279C>T ENSP00000306477.6:p.His427Tyr
ENST00000427382.2:c.1279C>T ENSP00000397113.2:p.His427Tyr
ENST00000437172.6:c.1279C>T ENSP00000400995.2:p.His427Tyr
ENST00000449107.7:c.1279C>T ENSP00000388212.2:p.His427Tyr
ENST00000643237.3:c.1279C>T MANE Select ENSP00000495254.2:p.His427Tyr
ENST00000646371.1:c.1279C>T ENSP00000495866.1:p.His427Tyr
ENST00000671928.1:c.165+3138C>T ENSP00000500069.1:n.165+3138C>T
ENST00000672065.1:c.1339C>T ENSP00000500403.1:p.His447Tyr
ENST00000672112.1:c.1345C>T ENSP00000500193.1:p.His449Tyr
ENST00000672141.1:c.399+3138C>T ENSP00000500210.1:n.399+3138C>T
ENST00000672427.1:c.1015+264C>T ENSP00000500131.1:n.1015+264C>T
ENST00000672760.1:c.399+3138C>T ENSP00000500530.1:n.399+3138C>T
ENST00000672892.1:c.793+264C>T ENSP00000499944.1:n.793+264C>T
ENST00000673467.1:c.399+3138C>T ENSP00000500288.1:n.399+3138C>T
ENST00000673620.1:c.399+3138C>T ENSP00000500325.1:n.399+3138C>T
ENST00000303498.9:c.1339C>T ENSP00000306477.5:p.His447Tyr
ENST00000383778.5:c.1279C>T ENSP00000373288.4:p.His427Tyr
ENST00000437172.5:c.1345C>T ENSP00000400995.1:p.His449Tyr
ENST00000449107.5:c.1345C>T ENSP00000388212.1:p.His449Tyr
NM_000060.3:c.1339C>T NP_000051.1:p.His447Tyr
NM_001281723.1:c.1345C>T NP_001268652.1:p.His449Tyr
NM_001281724.1:c.1345C>T NP_001268653.1:p.His449Tyr
NM_001281725.1:c.1279C>T NP_001268654.1:p.His427Tyr
XM_006713314.2:c.1279C>T XP_006713377.1:p.His427Tyr
XM_011534041.1:c.1279C>T XP_011532343.1:p.His427Tyr
NM_000060.4:c.1339C>T NP_000051.1:p.His447Tyr
NM_001281723.2:c.1345C>T NP_001268652.1:p.His449Tyr
NM_001281724.2:c.1345C>T NP_001268653.1:p.His449Tyr
NM_001281725.2:c.1279C>T NP_001268654.1:p.His427Tyr
NM_001323582.1:c.1279C>T NP_001310511.1:p.His427Tyr
XM_011534041.2:c.1279C>T XP_011532343.1:p.His427Tyr
XM_017007088.1:c.1279C>T XP_016862577.1:p.His427Tyr
XM_024453724.1:c.1279C>T XP_024309492.1:p.His427Tyr
NM_001281723.3:c.1279C>T NP_001268652.2:p.His427Tyr
NM_001281724.3:c.1279C>T NP_001268653.2:p.His427Tyr
NM_001370658.1:c.1279C>T MANE Select NP_001357587.1:p.His427Tyr
NM_001370752.1:c.1015+264C>T NP_001357681.1:n.1015+264C>T
NM_001370753.1:c.399+3138C>T NP_001357682.1:n.399+3138C>T
NM_001281726.2:c.*3057C>T NP_001268655.2:n.*3057C>T