Canonical Allele Identifier: CA1347655744

Gene: BTD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15602034_15602035delinsCT , CM000665.2:g.15602034_15602035delinsCT	GRCh38
NC_000003.11:g.15643541_15643542delinsCT , CM000665.1:g.15643541_15643542delinsCT	GRCh37
NC_000003.10:g.15618545_15618546delinsCT	NCBI36
NG_008019.1:g.5287_5288delinsCT
NG_008019.2:g.5683_5684delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436193.6:c.-293_-292delinsCT	ENSP00000394277.2:n.-293_-292delinsCT
ENST00000671928.2:c.-17+140_-17+141delinsCT	ENSP00000500069.2:n.-17+140_-17+141delinsCT
ENST00000672892.2:c.-17+140_-17+141delinsCT	ENSP00000499944.2:n.-17+140_-17+141delinsCT
ENST00000303498.10:c.-293+140_-293+141delinsCT	ENSP00000306477.6:n.-293+140_-293+141delinsCT
ENST00000417015.3:c.-17+140_-17+141delinsCT	ENSP00000403775.3:n.-17+140_-17+141delinsCT
ENST00000427382.2:c.-17+387_-17+388delinsCT	ENSP00000397113.2:n.-17+387_-17+388delinsCT
ENST00000437172.6:c.-205+140_-205+141delinsCT	ENSP00000400995.2:n.-205+140_-205+141delinsCT
ENST00000449107.7:c.-17+264_-17+265delinsCT	ENSP00000388212.2:n.-17+264_-17+265delinsCT
ENST00000467027.6:n.271_272delinsCT
ENST00000643237.3:c.-17+140_-17+141delinsCT MANE Select	ENSP00000495254.2:n.-17+140_-17+141delinsCT
ENST00000646371.1:c.-293+264_-293+265delinsCT	ENSP00000495866.1:n.-293+264_-293+265delinsCT
ENST00000672065.1:c.44+140_44+141delinsCT	ENSP00000500403.1:n.44+140_44+141delinsCT
ENST00000672112.1:c.-139+140_-139+141delinsCT	ENSP00000500193.1:n.-139+140_-139+141delinsCT
ENST00000672141.1:c.-17+140_-17+141delinsCT	ENSP00000500210.1:n.-17+140_-17+141delinsCT
ENST00000672336.1:c.-569_-568delinsCT	ENSP00000500267.1:n.-569_-568delinsCT
ENST00000672427.1:c.-17+140_-17+141delinsCT	ENSP00000500131.1:n.-17+140_-17+141delinsCT
ENST00000672760.1:c.-17+140_-17+141delinsCT	ENSP00000500530.1:n.-17+140_-17+141delinsCT
ENST00000672968.1:n.20+264_20+265delinsCT
ENST00000673467.1:c.-17+140_-17+141delinsCT	ENSP00000500288.1:n.-17+140_-17+141delinsCT
ENST00000673620.1:c.-17+264_-17+265delinsCT	ENSP00000500325.1:n.-17+264_-17+265delinsCT
ENST00000303498.9:c.44+140_44+141delinsCT	ENSP00000306477.5:n.44+140_44+141delinsCT
ENST00000383778.5:c.-293_-292delinsCT	ENSP00000373288.4:n.-293_-292delinsCT
ENST00000417015.1:c.*295+140_*295+141delinsCT	ENSP00000403775.1:n.*295+140_*295+141delinsCT
ENST00000427382.1:c.-17+387_-17+388delinsCT	ENSP00000397113.1:n.-17+387_-17+388delinsCT
ENST00000436193.5:c.-293_-292delinsCT	ENSP00000394277.1:n.-293_-292delinsCT
ENST00000437172.5:c.-139+140_-139+141delinsCT	ENSP00000400995.1:n.-139+140_-139+141delinsCT
ENST00000449107.5:c.50+264_50+265delinsCT	ENSP00000388212.1:n.50+264_50+265delinsCT
ENST00000467027.5:n.94+140_94+141delinsCT
ENST00000471964.5:n.125-103_125-102delinsCT
ENST00000480711.1:n.147+140_147+141delinsCT
ENST00000494021.1:n.401+264_401+265delinsCT
NM_000060.3:c.44+140_44+141delinsCT	NP_000051.1:n.44+140_44+141delinsCT
NM_001281723.1:c.50+264_50+265delinsCT	NP_001268652.1:n.50+264_50+265delinsCT
NM_001281724.1:c.-139+140_-139+141delinsCT	NP_001268653.1:n.-139+140_-139+141delinsCT
NM_001281725.1:c.-293_-292delinsCT	NP_001268654.1:n.-293_-292delinsCT
NM_001281726.1:c.44+140_44+141delinsCT	NP_001268655.1:n.44+140_44+141delinsCT
XM_006713314.2:c.-293+140_-293+141delinsCT	XP_006713377.1:n.-293+140_-293+141delinsCT
XM_011534041.1:c.-190-103_-190-102delinsCT	XP_011532343.1:n.-190-103_-190-102delinsCT
NM_000060.4:c.44+140_44+141delinsCT	NP_000051.1:n.44+140_44+141delinsCT
NM_001281723.2:c.50+264_50+265delinsCT	NP_001268652.1:n.50+264_50+265delinsCT
NM_001281724.2:c.-139+140_-139+141delinsCT	NP_001268653.1:n.-139+140_-139+141delinsCT
NM_001281725.2:c.-293_-292delinsCT	NP_001268654.1:n.-293_-292delinsCT
NM_001323582.1:c.-293+140_-293+141delinsCT	NP_001310511.1:n.-293+140_-293+141delinsCT
XM_011534041.2:c.-190-103_-190-102delinsCT	XP_011532343.1:n.-190-103_-190-102delinsCT
XM_017007088.1:c.-466-103_-466-102delinsCT	XP_016862577.1:n.-466-103_-466-102delinsCT
NM_001281723.3:c.-17+264_-17+265delinsCT	NP_001268652.2:n.-17+264_-17+265delinsCT
NM_001281724.3:c.-205+140_-205+141delinsCT	NP_001268653.2:n.-205+140_-205+141delinsCT
NM_001370658.1:c.-17+140_-17+141delinsCT MANE Select	NP_001357587.1:n.-17+140_-17+141delinsCT
NM_001370752.1:c.-17+140_-17+141delinsCT	NP_001357681.1:n.-17+140_-17+141delinsCT
NM_001370753.1:c.-17+140_-17+141delinsCT	NP_001357682.1:n.-17+140_-17+141delinsCT
NM_001281726.2:c.-17+140_-17+141delinsCT	NP_001268655.2:n.-17+140_-17+141delinsCT