Canonical Allele Identifier: CA1347655499

Gene: BTD HACL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601735C= , CM000665.2:g.15601735C=	GRCh38
NC_000003.11:g.15643242C= , CM000665.1:g.15643242C=	GRCh37
NC_000003.10:g.15618246C=	NCBI36
NG_008019.1:g.4988C=
NG_008019.2:g.5384C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-17+88C= (BTD)	ENSP00000397113.2:n.-17+88C=
ENST00000449107.7:c.-52C= (BTD)	ENSP00000388212.2:n.-52C=
ENST00000673620.1:c.-52C= (BTD)	ENSP00000500325.1:n.-52C=
ENST00000321169.9:c.-272G= (HACL1)	ENSP00000323811.5:n.-272G=
ENST00000417015.1:c.*136C= (BTD)	ENSP00000403775.1:n.*136C=
ENST00000427382.1:c.-17+88C= (BTD)	ENSP00000397113.1:n.-17+88C=
ENST00000449107.5:c.15C= (BTD)	ENSP00000388212.1:p.Gly5=
ENST00000494021.1:n.366C= (BTD)
ENST00000628377.2:c.-272G= (HACL1)	ENSP00000486684.1:n.-272G=
NM_001281723.1:c.15C= (BTD)	NP_001268652.1:p.Gly5=
NM_001284413.1:c.-272G= (HACL1)	NP_001271342.1:n.-272G=
NM_001284415.1:c.-272G= (HACL1)	NP_001271344.1:n.-272G=
NM_001284416.1:c.-272G= (HACL1)	NP_001271345.1:n.-272G=
NM_012260.3:c.-272G= (HACL1)	NP_036392.2:n.-272G=
NR_104315.1:n.118G= (HACL1)
NM_001281723.2:c.15C= (BTD)	NP_001268652.1:p.Gly5=
NM_001281723.3:c.-52C= (BTD)	NP_001268652.2:n.-52C=