Canonical Allele Identifier: CA274943
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

ClinVar Variation Id: 193740
dbSNP Id: rs794727006

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523512del , CM000673.2:g.66523512del GRCh38
NC_000011.9:g.66290983del , CM000673.1:g.66290983del GRCh37
NC_000011.8:g.66047559del NCBI36
NG_009093.1:g.17865del

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.887del (BBS1) MANE Select ENSP00000317469.7:p.Ile296ThrfsTer7
ENST00000318312.11:c.887del (BBS1) ENSP00000317469.7:p.Ile296ThrfsTer7
ENST00000393994.4:c.724-2611del (BBS1) ENSP00000377563.2:n.724-2611del
ENST00000419755.3:c.998del ENSP00000398526.3:p.Ile333ThrfsTer7
ENST00000455748.6:c.596del (BBS1) ENSP00000405764.2:p.Ile199ThrfsTer7
ENST00000524458.5:c.*676del (BBS1) ENSP00000436195.1:n.*676del
ENST00000524884.1:n.572del (BBS1)
ENST00000526760.5:c.*594del (BBS1) ENSP00000432140.1:n.*594del
ENST00000526986.5:c.*22-2046del (ZDHHC24) ENSP00000431321.1:n.*22-2046del
ENST00000527959.1:n.31del (BBS1)
ENST00000529766.5:n.894del (BBS1)
ENST00000529895.1:n.336del (BBS1)
ENST00000529955.5:n.858del (BBS1)
ENST00000532908.5:c.*547del (BBS1) ENSP00000431866.1:n.*547del
ENST00000533557.5:c.*741del (BBS1) ENSP00000434619.1:n.*741del
ENST00000533644.5:c.*345del (BBS1) ENSP00000436073.1:n.*345del
ENST00000534073.5:c.*143+643del (ZDHHC24) ENSP00000436503.1:n.*143+643del
ENST00000630659.2:c.*594del (BBS1) ENSP00000486455.1:n.*594del
NM_024649.4:c.887del (BBS1) NP_078925.3:p.Ile296ThrfsTer7
XM_005273874.3:c.*22-2046del (ZDHHC24) XP_005273931.1:n.*22-2046del
XR_949860.1:n.808+643del (ZDHHC24)
NM_001348571.1:c.*22-2046del (ZDHHC24) NP_001335500.1:n.*22-2046del
XM_005273874.4:c.*22-2046del (ZDHHC24) XP_005273931.1:n.*22-2046del
XR_001747823.2:n.862+643del (ZDHHC24)
XR_949860.3:n.933+643del (ZDHHC24)
NM_024649.5:c.887del (BBS1) MANE Select NP_078925.3:p.Ile296ThrfsTer7
NM_001348571.2:c.*22-2046del (ZDHHC24) NP_001335500.1:n.*22-2046del