Canonical Allele Identifier: CA901112963

Gene: BTD HACL1

Linked Data

• dbSNP Id: rs1171017405
• gnomAD v3: 3-15601656-G-A
• gnomAD v4: 3-15601656-G-A
• MyVariant Identifiers: chr3:g.15643163G>A (hg19) ; chr3:g.15601656G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601656G>A , CM000665.2:g.15601656G>A	GRCh38
NC_000003.11:g.15643163G>A , CM000665.1:g.15643163G>A	GRCh37
NC_000003.10:g.15618167G>A	NCBI36
NG_008019.1:g.4909G>A
NG_008019.2:g.5305G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-17+9G>A (BTD)	ENSP00000397113.2:n.-17+9G>A
ENST00000449107.7:c.-131G>A (BTD)	ENSP00000388212.2:n.-131G>A
ENST00000321169.9:c.-193C>T (HACL1)	ENSP00000323811.5:n.-193C>T
ENST00000417015.1:c.*57G>A (BTD)	ENSP00000403775.1:n.*57G>A
ENST00000427382.1:c.-17+9G>A (BTD)	ENSP00000397113.1:n.-17+9G>A
ENST00000449107.5:c.-65G>A (BTD)	ENSP00000388212.1:n.-65G>A
ENST00000494021.1:n.287G>A (BTD)
ENST00000628377.2:c.-193C>T (HACL1)	ENSP00000486684.1:n.-193C>T
NM_001281723.1:c.-65G>A (BTD)	NP_001268652.1:n.-65G>A
NM_001284413.1:c.-193C>T (HACL1)	NP_001271342.1:n.-193C>T
NM_001284415.1:c.-193C>T (HACL1)	NP_001271344.1:n.-193C>T
NM_001284416.1:c.-193C>T (HACL1)	NP_001271345.1:n.-193C>T
NM_012260.3:c.-193C>T (HACL1)	NP_036392.2:n.-193C>T
NR_104315.1:n.197C>T (HACL1)
NM_001281723.2:c.-65G>A (BTD)	NP_001268652.1:n.-65G>A
NM_001281723.3:c.-131G>A (BTD)	NP_001268652.2:n.-131G>A