Canonical Allele Identifier: CA1347655456

Gene: BTD HACL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601652G= , CM000665.2:g.15601652G=	GRCh38
NC_000003.11:g.15643159G= , CM000665.1:g.15643159G=	GRCh37
NC_000003.10:g.15618163G=	NCBI36
NG_008019.1:g.4905G=
NG_008019.2:g.5301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-17+5G= (BTD)	ENSP00000397113.2:n.-17+5G=
ENST00000449107.7:c.-135G= (BTD)	ENSP00000388212.2:n.-135G=
ENST00000321169.9:c.-189C= (HACL1)	ENSP00000323811.5:n.-189C=
ENST00000417015.1:c.*53G= (BTD)	ENSP00000403775.1:n.*53G=
ENST00000427382.1:c.-17+5G= (BTD)	ENSP00000397113.1:n.-17+5G=
ENST00000449107.5:c.-69G= (BTD)	ENSP00000388212.1:n.-69G=
ENST00000494021.1:n.283G= (BTD)
ENST00000628377.2:c.-189C= (HACL1)	ENSP00000486684.1:n.-189C=
NM_001281723.1:c.-69G= (BTD)	NP_001268652.1:n.-69G=
NM_001284413.1:c.-189C= (HACL1)	NP_001271342.1:n.-189C=
NM_001284415.1:c.-189C= (HACL1)	NP_001271344.1:n.-189C=
NM_001284416.1:c.-189C= (HACL1)	NP_001271345.1:n.-189C=
NM_012260.3:c.-189C= (HACL1)	NP_036392.2:n.-189C=
NR_104315.1:n.201C= (HACL1)
NM_001281723.2:c.-69G= (BTD)	NP_001268652.1:n.-69G=
NM_001281723.3:c.-135G= (BTD)	NP_001268652.2:n.-135G=