Canonical Allele Identifier: CA1139655729

Gene: BTD

Linked Data

• ClinVar Variation Id: 651913
• ClinVar RCV Id: RCV000807358
• dbSNP Id: rs2065654912

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15645032_15645034del , CM000665.2:g.15645032_15645034del	GRCh38
NC_000003.11:g.15686539_15686541del , CM000665.1:g.15686539_15686541del	GRCh37
NC_000003.10:g.15661543_15661545del	NCBI36
NG_008019.1:g.48285_48287del
NG_008019.2:g.48681_48683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436193.6:c.1116_1118del	ENSP00000394277.2:p.Thr373del
ENST00000671928.2:c.399+2975_399+2977del	ENSP00000500069.2:n.399+2975_399+2977del
ENST00000672892.2:c.1015+101_1015+103del	ENSP00000499944.2:n.1015+101_1015+103del
ENST00000303498.10:c.1116_1118del	ENSP00000306477.6:p.Thr373del
ENST00000427382.2:c.1116_1118del	ENSP00000397113.2:p.Thr373del
ENST00000437172.6:c.1116_1118del	ENSP00000400995.2:p.Thr373del
ENST00000449107.7:c.1116_1118del	ENSP00000388212.2:p.Thr373del
ENST00000643237.3:c.1116_1118del MANE Select	ENSP00000495254.2:p.Thr373del
ENST00000646371.1:c.1116_1118del	ENSP00000495866.1:p.Thr373del
ENST00000671928.1:c.165+2975_165+2977del	ENSP00000500069.1:n.165+2975_165+2977del
ENST00000672065.1:c.1176_1178del	ENSP00000500403.1:p.Thr393del
ENST00000672112.1:c.1182_1184del	ENSP00000500193.1:p.Thr395del
ENST00000672141.1:c.399+2975_399+2977del	ENSP00000500210.1:n.399+2975_399+2977del
ENST00000672427.1:c.1015+101_1015+103del	ENSP00000500131.1:n.1015+101_1015+103del
ENST00000672760.1:c.399+2975_399+2977del	ENSP00000500530.1:n.399+2975_399+2977del
ENST00000672892.1:c.793+101_793+103del	ENSP00000499944.1:n.793+101_793+103del
ENST00000673467.1:c.399+2975_399+2977del	ENSP00000500288.1:n.399+2975_399+2977del
ENST00000673620.1:c.399+2975_399+2977del	ENSP00000500325.1:n.399+2975_399+2977del
ENST00000303498.9:c.1176_1178del	ENSP00000306477.5:p.Thr393del
ENST00000383778.5:c.1116_1118del	ENSP00000373288.4:p.Thr373del
ENST00000437172.5:c.1182_1184del	ENSP00000400995.1:p.Thr395del
ENST00000449107.5:c.1182_1184del	ENSP00000388212.1:p.Thr395del
NM_000060.3:c.1176_1178del	NP_000051.1:p.Thr393del
NM_001281723.1:c.1182_1184del	NP_001268652.1:p.Thr395del
NM_001281724.1:c.1182_1184del	NP_001268653.1:p.Thr395del
NM_001281725.1:c.1116_1118del	NP_001268654.1:p.Thr373del
XM_006713314.2:c.1116_1118del	XP_006713377.1:p.Thr373del
XM_011534041.1:c.1116_1118del	XP_011532343.1:p.Thr373del
NM_000060.4:c.1176_1178del	NP_000051.1:p.Thr393del
NM_001281723.2:c.1182_1184del	NP_001268652.1:p.Thr395del
NM_001281724.2:c.1182_1184del	NP_001268653.1:p.Thr395del
NM_001281725.2:c.1116_1118del	NP_001268654.1:p.Thr373del
NM_001323582.1:c.1116_1118del	NP_001310511.1:p.Thr373del
XM_011534041.2:c.1116_1118del	XP_011532343.1:p.Thr373del
XM_017007088.1:c.1116_1118del	XP_016862577.1:p.Thr373del
XM_024453724.1:c.1116_1118del	XP_024309492.1:p.Thr373del
NM_001281723.3:c.1116_1118del	NP_001268652.2:p.Thr373del
NM_001281724.3:c.1116_1118del	NP_001268653.2:p.Thr373del
NM_001370658.1:c.1116_1118del MANE Select	NP_001357587.1:p.Thr373del
NM_001370752.1:c.1015+101_1015+103del	NP_001357681.1:n.1015+101_1015+103del
NM_001370753.1:c.399+2975_399+2977del	NP_001357682.1:n.399+2975_399+2977del
NM_001281726.2:c.*2894_*2896del	NP_001268655.2:n.*2894_*2896del