Canonical Allele Identifier: CA432649076

Gene: BTD

Linked Data

• MyVariant Identifiers: chr3:g.15643381C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601874C>T , CM000665.2:g.15601874C>T	GRCh38
NC_000003.11:g.15643381C>T , CM000665.1:g.15643381C>T	GRCh37
NC_000003.10:g.15618385C>T	NCBI36
NG_008019.1:g.5127C>T
NG_008019.2:g.5523C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000671928.2:c.-37C>T	ENSP00000500069.2:n.-37C>T
ENST00000672892.2:c.-37C>T	ENSP00000499944.2:n.-37C>T
ENST00000303498.10:c.-313C>T	ENSP00000306477.6:n.-313C>T
ENST00000417015.3:c.-37C>T	ENSP00000403775.3:n.-37C>T
ENST00000427382.2:c.-17+227C>T	ENSP00000397113.2:n.-17+227C>T
ENST00000437172.6:c.-225C>T	ENSP00000400995.2:n.-225C>T
ENST00000449107.7:c.-17+104C>T	ENSP00000388212.2:n.-17+104C>T
ENST00000467027.6:n.111C>T
ENST00000643237.3:c.-37C>T MANE Select	ENSP00000495254.2:n.-37C>T
ENST00000646371.1:c.-293+104C>T	ENSP00000495866.1:n.-293+104C>T
ENST00000672065.1:c.24C>T	ENSP00000500403.1:p.Gly8=
ENST00000672112.1:c.-159C>T	ENSP00000500193.1:n.-159C>T
ENST00000672141.1:c.-37C>T	ENSP00000500210.1:n.-37C>T
ENST00000672336.1:c.-729C>T	ENSP00000500267.1:n.-729C>T
ENST00000672427.1:c.-37C>T	ENSP00000500131.1:n.-37C>T
ENST00000672760.1:c.-37C>T	ENSP00000500530.1:n.-37C>T
ENST00000672968.1:n.20+104C>T
ENST00000673467.1:c.-37C>T	ENSP00000500288.1:n.-37C>T
ENST00000673620.1:c.-17+104C>T	ENSP00000500325.1:n.-17+104C>T
ENST00000303498.9:c.24C>T	ENSP00000306477.5:p.Gly8=
ENST00000417015.1:c.*275C>T	ENSP00000403775.1:n.*275C>T
ENST00000427382.1:c.-17+227C>T	ENSP00000397113.1:n.-17+227C>T
ENST00000437172.5:c.-159C>T	ENSP00000400995.1:n.-159C>T
ENST00000449107.5:c.50+104C>T	ENSP00000388212.1:n.50+104C>T
ENST00000467027.5:n.74C>T
ENST00000471964.5:n.104C>T
ENST00000480711.1:n.127C>T
ENST00000494021.1:n.401+104C>T
NM_000060.3:c.24C>T	NP_000051.1:p.Gly8=
NM_001281723.1:c.50+104C>T	NP_001268652.1:n.50+104C>T
NM_001281724.1:c.-159C>T	NP_001268653.1:n.-159C>T
NM_001281726.1:c.24C>T	NP_001268655.1:p.Gly8=
XM_006713314.2:c.-313C>T	XP_006713377.1:n.-313C>T
XM_011534041.1:c.-211C>T	XP_011532343.1:n.-211C>T
NM_000060.4:c.24C>T	NP_000051.1:p.Gly8=
NM_001281723.2:c.50+104C>T	NP_001268652.1:n.50+104C>T
NM_001281724.2:c.-159C>T	NP_001268653.1:n.-159C>T
NM_001323582.1:c.-313C>T	NP_001310511.1:n.-313C>T
XM_011534041.2:c.-211C>T	XP_011532343.1:n.-211C>T
XM_017007088.1:c.-487C>T	XP_016862577.1:n.-487C>T
NM_001281723.3:c.-17+104C>T	NP_001268652.2:n.-17+104C>T
NM_001281724.3:c.-225C>T	NP_001268653.2:n.-225C>T
NM_001370658.1:c.-37C>T MANE Select	NP_001357587.1:n.-37C>T
NM_001370752.1:c.-37C>T	NP_001357681.1:n.-37C>T
NM_001370753.1:c.-37C>T	NP_001357682.1:n.-37C>T
NM_001281726.2:c.-37C>T	NP_001268655.2:n.-37C>T