Canonical Allele Identifier: CA1347655409

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15601570G= , CM000665.2:g.15601570G= GRCh38
NC_000003.11:g.15643077G= , CM000665.1:g.15643077G= GRCh37
NC_000003.10:g.15618081G= NCBI36
NG_008019.1:g.4823G=
NG_008019.2:g.5219G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427382.2:c.-94G= (BTD) ENSP00000397113.2:n.-94G=
ENST00000449107.7:c.-217G= (BTD) ENSP00000388212.2:n.-217G=
ENST00000321169.9:c.-107C= (HACL1) ENSP00000323811.5:n.-107C=
ENST00000417015.1:c.166G= (BTD) ENSP00000403775.1:p.Asp56=
ENST00000421993.5:c.-107C= (HACL1) ENSP00000391393.1:n.-107C=
ENST00000427382.1:c.-94G= (BTD) ENSP00000397113.1:n.-94G=
ENST00000451445.6:c.-107C= (HACL1) ENSP00000403656.2:n.-107C=
ENST00000494021.1:n.201G= (BTD)
ENST00000628377.2:c.-107C= (HACL1) ENSP00000486684.1:n.-107C=
NM_001281723.1:c.-151G= (BTD) NP_001268652.1:n.-151G=
NM_001284413.1:c.-107C= (HACL1) NP_001271342.1:n.-107C=
NM_001284415.1:c.-107C= (HACL1) NP_001271344.1:n.-107C=
NM_001284416.1:c.-107C= (HACL1) NP_001271345.1:n.-107C=
NM_012260.3:c.-107C= (HACL1) NP_036392.2:n.-107C=
NR_104315.1:n.283C= (HACL1)
NM_001281723.2:c.-151G= (BTD) NP_001268652.1:n.-151G=
NM_001281723.3:c.-217G= (BTD) NP_001268652.2:n.-217G=