Canonical Allele Identifier: CA1979709878
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1856346688

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523629del , CM000673.2:g.66523629del GRCh38
NC_000011.9:g.66291100del , CM000673.1:g.66291100del GRCh37
NC_000011.8:g.66047676del NCBI36
NG_009093.1:g.17982del

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.951+53del (BBS1) MANE Select ENSP00000317469.7:n.951+53del
ENST00000318312.11:c.951+53del (BBS1) ENSP00000317469.7:n.951+53del
ENST00000393994.4:c.724-2494del (BBS1) ENSP00000377563.2:n.724-2494del
ENST00000419755.3:c.1062+53del ENSP00000398526.3:n.1062+53del
ENST00000455748.6:c.660+53del (BBS1) ENSP00000405764.2:n.660+53del
ENST00000526760.5:c.*658+53del (BBS1) ENSP00000432140.1:n.*658+53del
ENST00000526986.5:c.*22-2163del (ZDHHC24) ENSP00000431321.1:n.*22-2163del
ENST00000527959.1:n.95+53del (BBS1)
ENST00000529766.5:n.958+53del (BBS1)
ENST00000529895.1:n.400+53del (BBS1)
ENST00000529955.5:n.922+53del (BBS1)
ENST00000532908.5:c.*611+53del (BBS1) ENSP00000431866.1:n.*611+53del
ENST00000534073.5:c.*143+526del (ZDHHC24) ENSP00000436503.1:n.*143+526del
ENST00000630659.2:c.*658+53del (BBS1) ENSP00000486455.1:n.*658+53del
NM_024649.4:c.951+53del (BBS1) NP_078925.3:n.951+53del
XM_005273874.3:c.*22-2163del (ZDHHC24) XP_005273931.1:n.*22-2163del
XR_949860.1:n.808+526del (ZDHHC24)
NM_001348571.1:c.*22-2163del (ZDHHC24) NP_001335500.1:n.*22-2163del
XM_005273874.4:c.*22-2163del (ZDHHC24) XP_005273931.1:n.*22-2163del
XR_001747823.2:n.862+526del (ZDHHC24)
XR_949860.3:n.933+526del (ZDHHC24)
NM_024649.5:c.951+53del (BBS1) MANE Select NP_078925.3:n.951+53del
NM_001348571.2:c.*22-2163del (ZDHHC24) NP_001335500.1:n.*22-2163del