Canonical Allele Identifier: CA1347655534

Gene: BTD HACL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601786_15601788delinsCTG , CM000665.2:g.15601786_15601788delinsCTG	GRCh38
NC_000003.11:g.15643293_15643295delinsCTG , CM000665.1:g.15643293_15643295delinsCTG	GRCh37
NC_000003.10:g.15618297_15618299delinsCTG	NCBI36
NG_008019.1:g.5039_5041delinsCTG
NG_008019.2:g.5435_5437delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000671928.2:c.-125_-123delinsCTG (BTD)	ENSP00000500069.2:n.-125_-123delinsCTG
ENST00000672892.2:c.-125_-123delinsCTG (BTD)	ENSP00000499944.2:n.-125_-123delinsCTG
ENST00000303498.10:c.-401_-399delinsCTG (BTD)	ENSP00000306477.6:n.-401_-399delinsCTG
ENST00000417015.3:c.-125_-123delinsCTG (BTD)	ENSP00000403775.3:n.-125_-123delinsCTG
ENST00000427382.2:c.-17+139_-17+141delinsCTG (BTD)	ENSP00000397113.2:n.-17+139_-17+141delinsCTG
ENST00000449107.7:c.-17+16_-17+18delinsCTG (BTD)	ENSP00000388212.2:n.-17+16_-17+18delinsCTG
ENST00000467027.6:n.23_25delinsCTG (BTD)
ENST00000643237.3:c.-125_-123delinsCTG (BTD) MANE Select	ENSP00000495254.2:n.-125_-123delinsCTG
ENST00000646371.1:c.-293+16_-293+18delinsCTG (BTD)	ENSP00000495866.1:n.-293+16_-293+18delinsCTG
ENST00000672065.1:c.-65_-63delinsCTG (BTD)	ENSP00000500403.1:n.-65_-63delinsCTG
ENST00000672112.1:c.-247_-245delinsCTG (BTD)	ENSP00000500193.1:n.-247_-245delinsCTG
ENST00000672141.1:c.-125_-123delinsCTG (BTD)	ENSP00000500210.1:n.-125_-123delinsCTG
ENST00000672336.1:c.-817_-815delinsCTG (BTD)	ENSP00000500267.1:n.-817_-815delinsCTG
ENST00000672427.1:c.-125_-123delinsCTG (BTD)	ENSP00000500131.1:n.-125_-123delinsCTG
ENST00000672760.1:c.-125_-123delinsCTG (BTD)	ENSP00000500530.1:n.-125_-123delinsCTG
ENST00000672968.1:n.20+16_20+18delinsCTG (BTD)
ENST00000673467.1:c.-125_-123delinsCTG (BTD)	ENSP00000500288.1:n.-125_-123delinsCTG
ENST00000673620.1:c.-17+16_-17+18delinsCTG (BTD)	ENSP00000500325.1:n.-17+16_-17+18delinsCTG
ENST00000303498.9:c.-65_-63delinsCTG (BTD)	ENSP00000306477.5:n.-65_-63delinsCTG
ENST00000321169.9:c.-325_-323delinsCAG (HACL1)	ENSP00000323811.5:n.-325_-323delinsCAG
ENST00000417015.1:c.*187_*189delinsCTG (BTD)	ENSP00000403775.1:n.*187_*189delinsCTG
ENST00000427382.1:c.-17+139_-17+141delinsCTG (BTD)	ENSP00000397113.1:n.-17+139_-17+141delinsCTG
ENST00000449107.5:c.50+16_50+18delinsCTG (BTD)	ENSP00000388212.1:n.50+16_50+18delinsCTG
ENST00000471964.5:n.16_18delinsCTG (BTD)
ENST00000480711.1:n.39_41delinsCTG (BTD)
ENST00000494021.1:n.401+16_401+18delinsCTG (BTD)
ENST00000628377.2:c.-325_-323delinsCAG (HACL1)	ENSP00000486684.1:n.-325_-323delinsCAG
NM_000060.3:c.-65_-63delinsCTG (BTD)	NP_000051.1:n.-65_-63delinsCTG
NM_001281723.1:c.50+16_50+18delinsCTG (BTD)	NP_001268652.1:n.50+16_50+18delinsCTG
NM_001281724.1:c.-247_-245delinsCTG (BTD)	NP_001268653.1:n.-247_-245delinsCTG
NM_001281726.1:c.-65_-63delinsCTG (BTD)	NP_001268655.1:n.-65_-63delinsCTG
NM_001284413.1:c.-325_-323delinsCAG (HACL1)	NP_001271342.1:n.-325_-323delinsCAG
NM_001284415.1:c.-325_-323delinsCAG (HACL1)	NP_001271344.1:n.-325_-323delinsCAG
NM_001284416.1:c.-325_-323delinsCAG (HACL1)	NP_001271345.1:n.-325_-323delinsCAG
NM_012260.3:c.-325_-323delinsCAG (HACL1)	NP_036392.2:n.-325_-323delinsCAG
NR_104315.1:n.65_67delinsCAG (HACL1)
NM_000060.4:c.-65_-63delinsCTG (BTD)	NP_000051.1:n.-65_-63delinsCTG
NM_001281723.2:c.50+16_50+18delinsCTG (BTD)	NP_001268652.1:n.50+16_50+18delinsCTG
NM_001281724.2:c.-247_-245delinsCTG (BTD)	NP_001268653.1:n.-247_-245delinsCTG
NM_001323582.1:c.-401_-399delinsCTG (BTD)	NP_001310511.1:n.-401_-399delinsCTG
NM_001281723.3:c.-17+16_-17+18delinsCTG (BTD)	NP_001268652.2:n.-17+16_-17+18delinsCTG
NM_001281724.3:c.-313_-311delinsCTG (BTD)	NP_001268653.2:n.-313_-311delinsCTG
NM_001370658.1:c.-125_-123delinsCTG (BTD) MANE Select	NP_001357587.1:n.-125_-123delinsCTG
NM_001370752.1:c.-125_-123delinsCTG (BTD)	NP_001357681.1:n.-125_-123delinsCTG
NM_001370753.1:c.-125_-123delinsCTG (BTD)	NP_001357682.1:n.-125_-123delinsCTG
NM_001281726.2:c.-125_-123delinsCTG (BTD)	NP_001268655.2:n.-125_-123delinsCTG