Canonical Allele Identifier: CA2570954257

Gene: BTD HACL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601575A>G , CM000665.2:g.15601575A>G	GRCh38
NC_000003.11:g.15643082A>G , CM000665.1:g.15643082A>G	GRCh37
NC_000003.10:g.15618086A>G	NCBI36
NG_008019.1:g.4828A>G
NG_008019.2:g.5224A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-89A>G (BTD)	ENSP00000397113.2:n.-89A>G
ENST00000449107.7:c.-212A>G (BTD)	ENSP00000388212.2:n.-212A>G
ENST00000321169.9:c.-112T>C (HACL1)	ENSP00000323811.5:n.-112T>C
ENST00000417015.1:c.171A>G (BTD)	ENSP00000403775.1:p.Gly57=
ENST00000421993.5:c.-112T>C (HACL1)	ENSP00000391393.1:n.-112T>C
ENST00000427382.1:c.-89A>G (BTD)	ENSP00000397113.1:n.-89A>G
ENST00000451445.6:c.-112T>C (HACL1)	ENSP00000403656.2:n.-112T>C
ENST00000494021.1:n.206A>G (BTD)
ENST00000628377.2:c.-112T>C (HACL1)	ENSP00000486684.1:n.-112T>C
NM_001281723.1:c.-146A>G (BTD)	NP_001268652.1:n.-146A>G
NM_001284413.1:c.-112T>C (HACL1)	NP_001271342.1:n.-112T>C
NM_001284415.1:c.-112T>C (HACL1)	NP_001271344.1:n.-112T>C
NM_001284416.1:c.-112T>C (HACL1)	NP_001271345.1:n.-112T>C
NM_012260.3:c.-112T>C (HACL1)	NP_036392.2:n.-112T>C
NR_104315.1:n.278T>C (HACL1)
NM_001281723.2:c.-146A>G (BTD)	NP_001268652.1:n.-146A>G
NM_001281723.3:c.-212A>G (BTD)	NP_001268652.2:n.-212A>G