Canonical Allele Identifier: CA2664666306

Gene: BTD HACL1

Linked Data

• gnomAD v4: 3-15601618-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601618C>A , CM000665.2:g.15601618C>A	GRCh38
NC_000003.11:g.15643125C>A , CM000665.1:g.15643125C>A	GRCh37
NC_000003.10:g.15618129C>A	NCBI36
NG_008019.1:g.4871C>A
NG_008019.2:g.5267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-46C>A (BTD)	ENSP00000397113.2:n.-46C>A
ENST00000449107.7:c.-169C>A (BTD)	ENSP00000388212.2:n.-169C>A
ENST00000321169.9:c.-155G>T (HACL1)	ENSP00000323811.5:n.-155G>T
ENST00000417015.1:c.*19C>A (BTD)	ENSP00000403775.1:n.*19C>A
ENST00000427382.1:c.-46C>A (BTD)	ENSP00000397113.1:n.-46C>A
ENST00000494021.1:n.249C>A (BTD)
ENST00000628377.2:c.-155G>T (HACL1)	ENSP00000486684.1:n.-155G>T
NM_001281723.1:c.-103C>A (BTD)	NP_001268652.1:n.-103C>A
NM_001284413.1:c.-155G>T (HACL1)	NP_001271342.1:n.-155G>T
NM_001284415.1:c.-155G>T (HACL1)	NP_001271344.1:n.-155G>T
NM_001284416.1:c.-155G>T (HACL1)	NP_001271345.1:n.-155G>T
NM_012260.3:c.-155G>T (HACL1)	NP_036392.2:n.-155G>T
NR_104315.1:n.235G>T (HACL1)
NM_001281723.2:c.-103C>A (BTD)	NP_001268652.1:n.-103C>A
NM_001281723.3:c.-169C>A (BTD)	NP_001268652.2:n.-169C>A