Canonical Allele Identifier: CA1347655515

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15601757C= , CM000665.2:g.15601757C= GRCh38
NC_000003.11:g.15643264C= , CM000665.1:g.15643264C= GRCh37
NC_000003.10:g.15618268C= NCBI36
NG_008019.1:g.5010C=
NG_008019.2:g.5406C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000671928.2:c.-154C= (BTD) ENSP00000500069.2:n.-154C=
ENST00000672892.2:c.-154C= (BTD) ENSP00000499944.2:n.-154C=
ENST00000303498.10:c.-430C= (BTD) ENSP00000306477.6:n.-430C=
ENST00000417015.3:c.-154C= (BTD) ENSP00000403775.3:n.-154C=
ENST00000427382.2:c.-17+110C= (BTD) ENSP00000397113.2:n.-17+110C=
ENST00000449107.7:c.-30C= (BTD) ENSP00000388212.2:n.-30C=
ENST00000643237.3:c.-154C= (BTD) MANE Select ENSP00000495254.2:n.-154C=
ENST00000646371.1:c.-306C= (BTD) ENSP00000495866.1:n.-306C=
ENST00000672065.1:c.-94C= (BTD) ENSP00000500403.1:n.-94C=
ENST00000672112.1:c.-276C= (BTD) ENSP00000500193.1:n.-276C=
ENST00000672141.1:c.-154C= (BTD) ENSP00000500210.1:n.-154C=
ENST00000672968.1:n.7C= (BTD)
ENST00000673620.1:c.-30C= (BTD) ENSP00000500325.1:n.-30C=
ENST00000303498.9:c.-94C= (BTD) ENSP00000306477.5:n.-94C=
ENST00000321169.9:c.-294G= (HACL1) ENSP00000323811.5:n.-294G=
ENST00000417015.1:c.*158C= (BTD) ENSP00000403775.1:n.*158C=
ENST00000427382.1:c.-17+110C= (BTD) ENSP00000397113.1:n.-17+110C=
ENST00000449107.5:c.37C= (BTD) ENSP00000388212.1:p.Pro13=
ENST00000480711.1:n.10C= (BTD)
ENST00000494021.1:n.388C= (BTD)
ENST00000628377.2:c.-294G= (HACL1) ENSP00000486684.1:n.-294G=
NM_000060.3:c.-94C= (BTD) NP_000051.1:n.-94C=
NM_001281723.1:c.37C= (BTD) NP_001268652.1:p.Pro13=
NM_001281724.1:c.-276C= (BTD) NP_001268653.1:n.-276C=
NM_001281726.1:c.-94C= (BTD) NP_001268655.1:n.-94C=
NM_001284413.1:c.-294G= (HACL1) NP_001271342.1:n.-294G=
NM_001284415.1:c.-294G= (HACL1) NP_001271344.1:n.-294G=
NM_001284416.1:c.-294G= (HACL1) NP_001271345.1:n.-294G=
NM_012260.3:c.-294G= (HACL1) NP_036392.2:n.-294G=
NR_104315.1:n.96G= (HACL1)
NM_000060.4:c.-94C= (BTD) NP_000051.1:n.-94C=
NM_001281723.2:c.37C= (BTD) NP_001268652.1:p.Pro13=
NM_001281724.2:c.-276C= (BTD) NP_001268653.1:n.-276C=
NM_001323582.1:c.-430C= (BTD) NP_001310511.1:n.-430C=
NM_001281723.3:c.-30C= (BTD) NP_001268652.2:n.-30C=
NM_001281724.3:c.-342C= (BTD) NP_001268653.2:n.-342C=
NM_001370658.1:c.-154C= (BTD) MANE Select NP_001357587.1:n.-154C=
NM_001370752.1:c.-154C= (BTD) NP_001357681.1:n.-154C=
NM_001370753.1:c.-154C= (BTD) NP_001357682.1:n.-154C=
NM_001281726.2:c.-154C= (BTD) NP_001268655.2:n.-154C=