Canonical Allele Identifier: CA2577522517

Linked Data

gnomAD v4: 3-15601596-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15601596T>C , CM000665.2:g.15601596T>C GRCh38
NC_000003.11:g.15643103T>C , CM000665.1:g.15643103T>C GRCh37
NC_000003.10:g.15618107T>C NCBI36
NG_008019.1:g.4849T>C
NG_008019.2:g.5245T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000427382.2:c.-68T>C (BTD) ENSP00000397113.2:n.-68T>C
ENST00000449107.7:c.-191T>C (BTD) ENSP00000388212.2:n.-191T>C
ENST00000321169.9:c.-133A>G (HACL1) ENSP00000323811.5:n.-133A>G
ENST00000417015.1:c.192T>C (BTD) ENSP00000403775.1:p.Pro64=
ENST00000427382.1:c.-68T>C (BTD) ENSP00000397113.1:n.-68T>C
ENST00000494021.1:n.227T>C (BTD)
ENST00000628377.2:c.-133A>G (HACL1) ENSP00000486684.1:n.-133A>G
NM_001281723.1:c.-125T>C (BTD) NP_001268652.1:n.-125T>C
NM_001284413.1:c.-133A>G (HACL1) NP_001271342.1:n.-133A>G
NM_001284415.1:c.-133A>G (HACL1) NP_001271344.1:n.-133A>G
NM_001284416.1:c.-133A>G (HACL1) NP_001271345.1:n.-133A>G
NM_012260.3:c.-133A>G (HACL1) NP_036392.2:n.-133A>G
NR_104315.1:n.257A>G (HACL1)
NM_001281723.2:c.-125T>C (BTD) NP_001268652.1:n.-125T>C
NM_001281723.3:c.-191T>C (BTD) NP_001268652.2:n.-191T>C