Canonical Allele Identifier: CA1347655368

Gene: HACL1 BTD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601531G= , CM000665.2:g.15601531G=	GRCh38
NC_000003.11:g.15643038G= , CM000665.1:g.15643038G=	GRCh37
NC_000003.10:g.15618042G=	NCBI36
NG_008019.1:g.4784G=
NG_008019.2:g.5180G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321169.10:c.-68C= (HACL1) MANE Select	ENSP00000323811.5:n.-68C=
ENST00000427382.2:c.-133G= (BTD)	ENSP00000397113.2:n.-133G=
ENST00000449107.7:c.-256G= (BTD)	ENSP00000388212.2:n.-256G=
ENST00000321169.9:c.-68C= (HACL1)	ENSP00000323811.5:n.-68C=
ENST00000383779.8:c.-68C= (HACL1)	ENSP00000373289.4:n.-68C=
ENST00000414979.1:c.-68C= (HACL1)	ENSP00000395352.1:n.-68C=
ENST00000417015.1:c.127G= (BTD)	ENSP00000403775.1:p.Ala43=
ENST00000421993.5:c.-68C= (HACL1)	ENSP00000391393.1:n.-68C=
ENST00000422591.5:c.-68C= (HACL1)	ENSP00000392796.1:n.-68C=
ENST00000427382.1:c.-133G= (BTD)	ENSP00000397113.1:n.-133G=
ENST00000435217.6:c.-68C= (HACL1)	ENSP00000395278.2:n.-68C=
ENST00000451445.6:c.-68C= (HACL1)	ENSP00000403656.2:n.-68C=
ENST00000456194.6:c.-68C= (HACL1)	ENSP00000390699.2:n.-68C=
ENST00000457447.6:c.-68C= (HACL1)	ENSP00000404883.2:n.-68C=
ENST00000460907.1:n.39C= (HACL1)
ENST00000472857.1:n.16C= (HACL1)
ENST00000494021.1:n.162G= (BTD)
ENST00000628377.2:c.-68C= (HACL1)	ENSP00000486684.1:n.-68C=
NM_001281723.1:c.-190G= (BTD)	NP_001268652.1:n.-190G=
NM_001284413.1:c.-68C= (HACL1)	NP_001271342.1:n.-68C=
NM_001284415.1:c.-68C= (HACL1)	NP_001271344.1:n.-68C=
NM_001284416.1:c.-68C= (HACL1)	NP_001271345.1:n.-68C=
NM_012260.3:c.-68C= (HACL1)	NP_036392.2:n.-68C=
NR_104315.1:n.322C= (HACL1)
NM_001281723.2:c.-190G= (BTD)	NP_001268652.1:n.-190G=
NM_001281723.3:c.-256G= (BTD)	NP_001268652.2:n.-256G=
NM_001284413.2:c.-68C= (HACL1)	NP_001271342.1:n.-68C=
NM_001284415.2:c.-68C= (HACL1)	NP_001271344.1:n.-68C=
NM_001284416.2:c.-68C= (HACL1)	NP_001271345.1:n.-68C=
NM_012260.4:c.-68C= (HACL1) MANE Select	NP_036392.2:n.-68C=
NR_104315.2:n.39C= (HACL1)