Canonical Allele Identifier: CA1347655434

Gene: BTD HACL1

Linked Data

• dbSNP Id: rs2064245567

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15601604C>G , CM000665.2:g.15601604C>G	GRCh38
NC_000003.11:g.15643111C>G , CM000665.1:g.15643111C>G	GRCh37
NC_000003.10:g.15618115C>G	NCBI36
NG_008019.1:g.4857C>G
NG_008019.2:g.5253C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427382.2:c.-60C>G (BTD)	ENSP00000397113.2:n.-60C>G
ENST00000449107.7:c.-183C>G (BTD)	ENSP00000388212.2:n.-183C>G
ENST00000321169.9:c.-141G>C (HACL1)	ENSP00000323811.5:n.-141G>C
ENST00000417015.1:c.*5C>G (BTD)	ENSP00000403775.1:n.*5C>G
ENST00000427382.1:c.-60C>G (BTD)	ENSP00000397113.1:n.-60C>G
ENST00000494021.1:n.235C>G (BTD)
ENST00000628377.2:c.-141G>C (HACL1)	ENSP00000486684.1:n.-141G>C
NM_001281723.1:c.-117C>G (BTD)	NP_001268652.1:n.-117C>G
NM_001284413.1:c.-141G>C (HACL1)	NP_001271342.1:n.-141G>C
NM_001284415.1:c.-141G>C (HACL1)	NP_001271344.1:n.-141G>C
NM_001284416.1:c.-141G>C (HACL1)	NP_001271345.1:n.-141G>C
NM_012260.3:c.-141G>C (HACL1)	NP_036392.2:n.-141G>C
NR_104315.1:n.249G>C (HACL1)
NM_001281723.2:c.-117C>G (BTD)	NP_001268652.1:n.-117C>G
NM_001281723.3:c.-183C>G (BTD)	NP_001268652.2:n.-183C>G