Canonical Allele Identifier: CA1979709964
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523781G= , CM000673.2:g.66523781G= GRCh38
NC_000011.9:g.66291252G= , CM000673.1:g.66291252G= GRCh37
NC_000011.8:g.66047828G= NCBI36
NG_009093.1:g.18134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1009G= (BBS1) MANE Select ENSP00000317469.7:p.Glu337=
ENST00000318312.11:c.1009G= (BBS1) ENSP00000317469.7:p.Glu337=
ENST00000393994.4:c.724-2342G= (BBS1) ENSP00000377563.2:n.724-2342G=
ENST00000419755.3:c.1120G= ENSP00000398526.3:p.Glu374=
ENST00000455748.6:c.718G= (BBS1) ENSP00000405764.2:p.Glu240=
ENST00000526760.5:c.*716G= (BBS1) ENSP00000432140.1:n.*716G=
ENST00000526986.5:c.*22-2315C= (ZDHHC24) ENSP00000431321.1:n.*22-2315C=
ENST00000527959.1:n.153G= (BBS1)
ENST00000529766.5:n.1016G= (BBS1)
ENST00000529895.1:n.458G= (BBS1)
ENST00000529955.5:n.980G= (BBS1)
ENST00000532908.5:c.*669G= (BBS1) ENSP00000431866.1:n.*669G=
ENST00000534073.5:c.*143+374C= (ZDHHC24) ENSP00000436503.1:n.*143+374C=
ENST00000630659.2:c.*716G= (BBS1) ENSP00000486455.1:n.*716G=
NM_024649.4:c.1009G= (BBS1) NP_078925.3:p.Glu337=
XM_005273874.3:c.*22-2315C= (ZDHHC24) XP_005273931.1:n.*22-2315C=
XR_949860.1:n.808+374C= (ZDHHC24)
NM_001348571.1:c.*22-2315C= (ZDHHC24) NP_001335500.1:n.*22-2315C=
XM_005273874.4:c.*22-2315C= (ZDHHC24) XP_005273931.1:n.*22-2315C=
XR_001747823.2:n.862+374C= (ZDHHC24)
XR_949860.3:n.933+374C= (ZDHHC24)
NM_024649.5:c.1009G= (BBS1) MANE Select NP_078925.3:p.Glu337=
NM_001348571.2:c.*22-2315C= (ZDHHC24) NP_001335500.1:n.*22-2315C=