Canonical Allele Identifier: CA16604827

Gene: BTD

Linked Data

• ClinVar Variation Id: 379232
• ClinVar RCV Id: RCV000428786 ; RCV000675056
• dbSNP Id: rs1057520533
• MyVariant Identifiers: chr3:g.15686229C>T (hg19) ; chr3:g.15644722C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15644722C>T , CM000665.2:g.15644722C>T	GRCh38
NC_000003.11:g.15686229C>T , CM000665.1:g.15686229C>T	GRCh37
NC_000003.10:g.15661233C>T	NCBI36
NG_008019.1:g.47975C>T
NG_008019.2:g.48371C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436193.6:c.806C>T	ENSP00000394277.2:p.Ala269Val
ENST00000671928.2:c.399+2665C>T	ENSP00000500069.2:n.399+2665C>T
ENST00000672892.2:c.806C>T	ENSP00000499944.2:p.Ala269Val
ENST00000303498.10:c.806C>T	ENSP00000306477.6:p.Ala269Val
ENST00000427382.2:c.806C>T	ENSP00000397113.2:p.Ala269Val
ENST00000437172.6:c.806C>T	ENSP00000400995.2:p.Ala269Val
ENST00000449107.7:c.806C>T	ENSP00000388212.2:p.Ala269Val
ENST00000643237.3:c.806C>T MANE Select	ENSP00000495254.2:p.Ala269Val
ENST00000646371.1:c.806C>T	ENSP00000495866.1:p.Ala269Val
ENST00000671928.1:c.165+2665C>T	ENSP00000500069.1:n.165+2665C>T
ENST00000672065.1:c.866C>T	ENSP00000500403.1:p.Ala289Val
ENST00000672112.1:c.872C>T	ENSP00000500193.1:p.Ala291Val
ENST00000672141.1:c.399+2665C>T	ENSP00000500210.1:n.399+2665C>T
ENST00000672427.1:c.806C>T	ENSP00000500131.1:p.Ala269Val
ENST00000672760.1:c.399+2665C>T	ENSP00000500530.1:n.399+2665C>T
ENST00000672892.1:c.584C>T	ENSP00000499944.1:p.Ala195Val
ENST00000673467.1:c.399+2665C>T	ENSP00000500288.1:n.399+2665C>T
ENST00000673620.1:c.399+2665C>T	ENSP00000500325.1:n.399+2665C>T
ENST00000303498.9:c.866C>T	ENSP00000306477.5:p.Ala289Val
ENST00000383778.5:c.806C>T	ENSP00000373288.4:p.Ala269Val
ENST00000437172.5:c.872C>T	ENSP00000400995.1:p.Ala291Val
ENST00000449107.5:c.872C>T	ENSP00000388212.1:p.Ala291Val
NM_000060.3:c.866C>T	NP_000051.1:p.Ala289Val
NM_001281723.1:c.872C>T	NP_001268652.1:p.Ala291Val
NM_001281724.1:c.872C>T	NP_001268653.1:p.Ala291Val
NM_001281725.1:c.806C>T	NP_001268654.1:p.Ala269Val
XM_006713314.2:c.806C>T	XP_006713377.1:p.Ala269Val
XM_011534041.1:c.806C>T	XP_011532343.1:p.Ala269Val
NM_000060.4:c.866C>T	NP_000051.1:p.Ala289Val
NM_001281723.2:c.872C>T	NP_001268652.1:p.Ala291Val
NM_001281724.2:c.872C>T	NP_001268653.1:p.Ala291Val
NM_001281725.2:c.806C>T	NP_001268654.1:p.Ala269Val
NM_001323582.1:c.806C>T	NP_001310511.1:p.Ala269Val
XM_011534041.2:c.806C>T	XP_011532343.1:p.Ala269Val
XM_017007088.1:c.806C>T	XP_016862577.1:p.Ala269Val
XM_024453724.1:c.806C>T	XP_024309492.1:p.Ala269Val
NM_001281723.3:c.806C>T	NP_001268652.2:p.Ala269Val
NM_001281724.3:c.806C>T	NP_001268653.2:p.Ala269Val
NM_001370658.1:c.806C>T MANE Select	NP_001357587.1:p.Ala269Val
NM_001370752.1:c.806C>T	NP_001357681.1:p.Ala269Val
NM_001370753.1:c.399+2665C>T	NP_001357682.1:n.399+2665C>T
NM_001281726.2:c.*2584C>T	NP_001268655.2:n.*2584C>T