Canonical Allele Identifier: CA1979711971
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526771G= , CM000673.2:g.66526771G= GRCh38
NC_000011.9:g.66294242G= , CM000673.1:g.66294242G= GRCh37
NC_000011.8:g.66050818G= NCBI36
NG_009093.1:g.21124G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1303G= (BBS1) MANE Select ENSP00000317469.7:p.Val435=
ENST00000318312.11:c.1303G= (BBS1) ENSP00000317469.7:p.Val435=
ENST00000393994.4:c.916G= (BBS1) ENSP00000377563.2:p.Val306=
ENST00000419755.3:c.1414G= ENSP00000398526.3:p.Val472=
ENST00000455748.6:c.1012G= (BBS1) ENSP00000405764.2:p.Val338=
ENST00000526760.5:c.*1010G= (BBS1) ENSP00000432140.1:n.*1010G=
ENST00000526986.5:c.*21+165C= (ZDHHC24) ENSP00000431321.1:n.*21+165C=
ENST00000527959.1:n.447G= (BBS1)
ENST00000529766.5:n.1310G= (BBS1)
ENST00000529955.5:n.1274G= (BBS1)
ENST00000534073.5:c.*21+165C= (ZDHHC24) ENSP00000436503.1:n.*21+165C=
ENST00000630659.2:c.*1010G= (BBS1) ENSP00000486455.1:n.*1010G=
NM_024649.4:c.1303G= (BBS1) NP_078925.3:p.Val435=
XM_005273874.3:c.*21+165C= (ZDHHC24) XP_005273931.1:n.*21+165C=
XM_011544894.1:c.*21+165C= (ZDHHC24) XP_011543196.1:n.*21+165C=
XM_011544895.1:c.560-2495C= (ZDHHC24) XP_011543197.1:n.560-2495C=
XR_949860.1:n.686+165C= (ZDHHC24)
NM_001348571.1:c.*21+165C= (ZDHHC24) NP_001335500.1:n.*21+165C=
XM_005273874.4:c.*21+165C= (ZDHHC24) XP_005273931.1:n.*21+165C=
XM_011544894.2:c.*21+165C= (ZDHHC24) XP_011543196.1:n.*21+165C=
XR_001747823.2:n.741-2495C= (ZDHHC24)
XR_949860.3:n.811+165C= (ZDHHC24)
NM_024649.5:c.1303G= (BBS1) MANE Select NP_078925.3:p.Val435=
NM_001348571.2:c.*21+165C= (ZDHHC24) NP_001335500.1:n.*21+165C=