Canonical Allele Identifier: CA1347665630
Gene: BTD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15645309_15645329delinsCACCTGTGGGGCAACTTCAGT , CM000665.2:g.15645309_15645329delinsCACCTGTGGGGCAACTTCAGT GRCh38
NC_000003.11:g.15686816_15686836delinsCACCTGTGGGGCAACTTCAGT , CM000665.1:g.15686816_15686836delinsCACCTGTGGGGCAACTTCAGT GRCh37
NC_000003.10:g.15661820_15661840delinsCACCTGTGGGGCAACTTCAGT NCBI36
NG_008019.1:g.48562_48582delinsCACCTGTGGGGCAACTTCAGT
NG_008019.2:g.48958_48978delinsCACCTGTGGGGCAACTTCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000436193.6:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000394277.2:p.His465=
ENST00000671928.2:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500069.2:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTC...
ENST00000672892.2:c.1015+378_1015+398delinsCACCTGTGGGGCAACTTCAGT ENSP00000499944.2:n.1015+378_1015+398delinsCACCTGTGGGGCAACTTC...
ENST00000303498.10:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000306477.6:p.His465=
ENST00000427382.2:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000397113.2:p.His465=
ENST00000437172.6:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000400995.2:p.His465=
ENST00000449107.7:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000388212.2:p.His465=
ENST00000643237.3:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT MANE Select ENSP00000495254.2:p.His465=
ENST00000646371.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000495866.1:p.His465=
ENST00000671928.1:c.165+3252_165+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500069.1:n.165+3252_165+3272delinsCACCTGTGGGGCAACTTC...
ENST00000672065.1:c.1453_1473delinsCACCTGTGGGGCAACTTCAGT ENSP00000500403.1:p.His485=
ENST00000672112.1:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT ENSP00000500193.1:p.His487=
ENST00000672141.1:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500210.1:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTC...
ENST00000672427.1:c.1015+378_1015+398delinsCACCTGTGGGGCAACTTCAGT ENSP00000500131.1:n.1015+378_1015+398delinsCACCTGTGGGGCAACTTC...
ENST00000672760.1:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500530.1:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTC...
ENST00000672892.1:c.793+378_793+398delinsCACCTGTGGGGCAACTTCAGT ENSP00000499944.1:n.793+378_793+398delinsCACCTGTGGGGCAACTTCAG...
ENST00000673467.1:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500288.1:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTC...
ENST00000673620.1:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT ENSP00000500325.1:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTC...
ENST00000303498.9:c.1453_1473delinsCACCTGTGGGGCAACTTCAGT ENSP00000306477.5:p.His485=
ENST00000383778.5:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT ENSP00000373288.4:p.His465=
ENST00000437172.5:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT ENSP00000400995.1:p.His487=
ENST00000449107.5:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT ENSP00000388212.1:p.His487=
NM_000060.3:c.1453_1473delinsCACCTGTGGGGCAACTTCAGT NP_000051.1:p.His485=
NM_001281723.1:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT NP_001268652.1:p.His487=
NM_001281724.1:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT NP_001268653.1:p.His487=
NM_001281725.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT NP_001268654.1:p.His465=
XM_006713314.2:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT XP_006713377.1:p.His465=
XM_011534041.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT XP_011532343.1:p.His465=
NM_000060.4:c.1453_1473delinsCACCTGTGGGGCAACTTCAGT NP_000051.1:p.His485=
NM_001281723.2:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT NP_001268652.1:p.His487=
NM_001281724.2:c.1459_1479delinsCACCTGTGGGGCAACTTCAGT NP_001268653.1:p.His487=
NM_001281725.2:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT NP_001268654.1:p.His465=
NM_001323582.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT NP_001310511.1:p.His465=
XM_011534041.2:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT XP_011532343.1:p.His465=
XM_017007088.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT XP_016862577.1:p.His465=
XM_024453724.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT XP_024309492.1:p.His465=
NM_001281723.3:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT NP_001268652.2:p.His465=
NM_001281724.3:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT NP_001268653.2:p.His465=
NM_001370658.1:c.1393_1413delinsCACCTGTGGGGCAACTTCAGT MANE Select NP_001357587.1:p.His465=
NM_001370752.1:c.1015+378_1015+398delinsCACCTGTGGGGCAACTTCAGT NP_001357681.1:n.1015+378_1015+398delinsCACCTGTGGGGCAACTTCAGT...
NM_001370753.1:c.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT NP_001357682.1:n.399+3252_399+3272delinsCACCTGTGGGGCAACTTCAGT...
NM_001281726.2:c.*3171_*3191delinsCACCTGTGGGGCAACTTCAGT NP_001268655.2:n.*3171_*3191delinsCACCTGTGGGGCAACTTCAGT