Canonical Allele Identifier: CA1979711906
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526734C= , CM000673.2:g.66526734C= GRCh38
NC_000011.9:g.66294205C= , CM000673.1:g.66294205C= GRCh37
NC_000011.8:g.66050781C= NCBI36
NG_009093.1:g.21087C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1266C= (BBS1) MANE Select ENSP00000317469.7:p.Ala422=
ENST00000318312.11:c.1266C= (BBS1) ENSP00000317469.7:p.Ala422=
ENST00000393994.4:c.879C= (BBS1) ENSP00000377563.2:p.Ala293=
ENST00000419755.3:c.1377C= ENSP00000398526.3:p.Ala459=
ENST00000455748.6:c.975C= (BBS1) ENSP00000405764.2:p.Ala325=
ENST00000526760.5:c.*973C= (BBS1) ENSP00000432140.1:n.*973C=
ENST00000526986.5:c.*21+202G= (ZDHHC24) ENSP00000431321.1:n.*21+202G=
ENST00000527959.1:n.410C= (BBS1)
ENST00000529766.5:n.1273C= (BBS1)
ENST00000529955.5:n.1237C= (BBS1)
ENST00000534073.5:c.*21+202G= (ZDHHC24) ENSP00000436503.1:n.*21+202G=
ENST00000630659.2:c.*973C= (BBS1) ENSP00000486455.1:n.*973C=
NM_024649.4:c.1266C= (BBS1) NP_078925.3:p.Ala422=
XM_005273874.3:c.*21+202G= (ZDHHC24) XP_005273931.1:n.*21+202G=
XM_011544894.1:c.*21+202G= (ZDHHC24) XP_011543196.1:n.*21+202G=
XM_011544895.1:c.560-2458G= (ZDHHC24) XP_011543197.1:n.560-2458G=
XR_949860.1:n.686+202G= (ZDHHC24)
NM_001348571.1:c.*21+202G= (ZDHHC24) NP_001335500.1:n.*21+202G=
XM_005273874.4:c.*21+202G= (ZDHHC24) XP_005273931.1:n.*21+202G=
XM_011544894.2:c.*21+202G= (ZDHHC24) XP_011543196.1:n.*21+202G=
XR_001747823.2:n.741-2458G= (ZDHHC24)
XR_949860.3:n.811+202G= (ZDHHC24)
NM_024649.5:c.1266C= (BBS1) MANE Select NP_078925.3:p.Ala422=
NM_001348571.2:c.*21+202G= (ZDHHC24) NP_001335500.1:n.*21+202G=