Canonical Allele Identifier: CA1347655661

Gene: BTD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601922_15601923delinsAG , CM000665.2:g.15601922_15601923delinsAG	GRCh38
NC_000003.11:g.15643429_15643430delinsAG , CM000665.1:g.15643429_15643430delinsAG	GRCh37
NC_000003.10:g.15618433_15618434delinsAG	NCBI36
NG_008019.1:g.5175_5176delinsAG
NG_008019.2:g.5571_5572delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000671928.2:c.-17+28_-17+29delinsAG	ENSP00000500069.2:n.-17+28_-17+29delinsAG
ENST00000672892.2:c.-17+28_-17+29delinsAG	ENSP00000499944.2:n.-17+28_-17+29delinsAG
ENST00000303498.10:c.-293+28_-293+29delinsAG	ENSP00000306477.6:n.-293+28_-293+29delinsAG
ENST00000417015.3:c.-17+28_-17+29delinsAG	ENSP00000403775.3:n.-17+28_-17+29delinsAG
ENST00000427382.2:c.-17+275_-17+276delinsAG	ENSP00000397113.2:n.-17+275_-17+276delinsAG
ENST00000437172.6:c.-205+28_-205+29delinsAG	ENSP00000400995.2:n.-205+28_-205+29delinsAG
ENST00000449107.7:c.-17+152_-17+153delinsAG	ENSP00000388212.2:n.-17+152_-17+153delinsAG
ENST00000467027.6:n.159_160delinsAG
ENST00000643237.3:c.-17+28_-17+29delinsAG MANE Select	ENSP00000495254.2:n.-17+28_-17+29delinsAG
ENST00000646371.1:c.-293+152_-293+153delinsAG	ENSP00000495866.1:n.-293+152_-293+153delinsAG
ENST00000672065.1:c.44+28_44+29delinsAG	ENSP00000500403.1:n.44+28_44+29delinsAG
ENST00000672112.1:c.-139+28_-139+29delinsAG	ENSP00000500193.1:n.-139+28_-139+29delinsAG
ENST00000672141.1:c.-17+28_-17+29delinsAG	ENSP00000500210.1:n.-17+28_-17+29delinsAG
ENST00000672336.1:c.-681_-680delinsAG	ENSP00000500267.1:n.-681_-680delinsAG
ENST00000672427.1:c.-17+28_-17+29delinsAG	ENSP00000500131.1:n.-17+28_-17+29delinsAG
ENST00000672760.1:c.-17+28_-17+29delinsAG	ENSP00000500530.1:n.-17+28_-17+29delinsAG
ENST00000672968.1:n.20+152_20+153delinsAG
ENST00000673467.1:c.-17+28_-17+29delinsAG	ENSP00000500288.1:n.-17+28_-17+29delinsAG
ENST00000673620.1:c.-17+152_-17+153delinsAG	ENSP00000500325.1:n.-17+152_-17+153delinsAG
ENST00000303498.9:c.44+28_44+29delinsAG	ENSP00000306477.5:n.44+28_44+29delinsAG
ENST00000417015.1:c.*295+28_*295+29delinsAG	ENSP00000403775.1:n.*295+28_*295+29delinsAG
ENST00000427382.1:c.-17+275_-17+276delinsAG	ENSP00000397113.1:n.-17+275_-17+276delinsAG
ENST00000437172.5:c.-139+28_-139+29delinsAG	ENSP00000400995.1:n.-139+28_-139+29delinsAG
ENST00000449107.5:c.50+152_50+153delinsAG	ENSP00000388212.1:n.50+152_50+153delinsAG
ENST00000467027.5:n.94+28_94+29delinsAG
ENST00000471964.5:n.124+28_124+29delinsAG
ENST00000480711.1:n.147+28_147+29delinsAG
ENST00000494021.1:n.401+152_401+153delinsAG
NM_000060.3:c.44+28_44+29delinsAG	NP_000051.1:n.44+28_44+29delinsAG
NM_001281723.1:c.50+152_50+153delinsAG	NP_001268652.1:n.50+152_50+153delinsAG
NM_001281724.1:c.-139+28_-139+29delinsAG	NP_001268653.1:n.-139+28_-139+29delinsAG
NM_001281726.1:c.44+28_44+29delinsAG	NP_001268655.1:n.44+28_44+29delinsAG
XM_006713314.2:c.-293+28_-293+29delinsAG	XP_006713377.1:n.-293+28_-293+29delinsAG
XM_011534041.1:c.-191+28_-191+29delinsAG	XP_011532343.1:n.-191+28_-191+29delinsAG
NM_000060.4:c.44+28_44+29delinsAG	NP_000051.1:n.44+28_44+29delinsAG
NM_001281723.2:c.50+152_50+153delinsAG	NP_001268652.1:n.50+152_50+153delinsAG
NM_001281724.2:c.-139+28_-139+29delinsAG	NP_001268653.1:n.-139+28_-139+29delinsAG
NM_001323582.1:c.-293+28_-293+29delinsAG	NP_001310511.1:n.-293+28_-293+29delinsAG
XM_011534041.2:c.-191+28_-191+29delinsAG	XP_011532343.1:n.-191+28_-191+29delinsAG
XM_017007088.1:c.-467+28_-467+29delinsAG	XP_016862577.1:n.-467+28_-467+29delinsAG
NM_001281723.3:c.-17+152_-17+153delinsAG	NP_001268652.2:n.-17+152_-17+153delinsAG
NM_001281724.3:c.-205+28_-205+29delinsAG	NP_001268653.2:n.-205+28_-205+29delinsAG
NM_001370658.1:c.-17+28_-17+29delinsAG MANE Select	NP_001357587.1:n.-17+28_-17+29delinsAG
NM_001370752.1:c.-17+28_-17+29delinsAG	NP_001357681.1:n.-17+28_-17+29delinsAG
NM_001370753.1:c.-17+28_-17+29delinsAG	NP_001357682.1:n.-17+28_-17+29delinsAG
NM_001281726.2:c.-17+28_-17+29delinsAG	NP_001268655.2:n.-17+28_-17+29delinsAG