Canonical Allele Identifier: CA1979709901
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523669G= , CM000673.2:g.66523669G= GRCh38
NC_000011.9:g.66291140G= , CM000673.1:g.66291140G= GRCh37
NC_000011.8:g.66047716G= NCBI36
NG_009093.1:g.18022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.952-55G= (BBS1) MANE Select ENSP00000317469.7:n.952-55G=
ENST00000318312.11:c.952-55G= (BBS1) ENSP00000317469.7:n.952-55G=
ENST00000393994.4:c.724-2454G= (BBS1) ENSP00000377563.2:n.724-2454G=
ENST00000419755.3:c.1063-55G= ENSP00000398526.3:n.1063-55G=
ENST00000455748.6:c.661-55G= (BBS1) ENSP00000405764.2:n.661-55G=
ENST00000526760.5:c.*659-55G= (BBS1) ENSP00000432140.1:n.*659-55G=
ENST00000526986.5:c.*22-2203C= (ZDHHC24) ENSP00000431321.1:n.*22-2203C=
ENST00000527959.1:n.96-55G= (BBS1)
ENST00000529766.5:n.959-55G= (BBS1)
ENST00000529895.1:n.401-55G= (BBS1)
ENST00000529955.5:n.923-55G= (BBS1)
ENST00000532908.5:c.*612-55G= (BBS1) ENSP00000431866.1:n.*612-55G=
ENST00000534073.5:c.*143+486C= (ZDHHC24) ENSP00000436503.1:n.*143+486C=
ENST00000630659.2:c.*659-55G= (BBS1) ENSP00000486455.1:n.*659-55G=
NM_024649.4:c.952-55G= (BBS1) NP_078925.3:n.952-55G=
XM_005273874.3:c.*22-2203C= (ZDHHC24) XP_005273931.1:n.*22-2203C=
XR_949860.1:n.808+486C= (ZDHHC24)
NM_001348571.1:c.*22-2203C= (ZDHHC24) NP_001335500.1:n.*22-2203C=
XM_005273874.4:c.*22-2203C= (ZDHHC24) XP_005273931.1:n.*22-2203C=
XR_001747823.2:n.862+486C= (ZDHHC24)
XR_949860.3:n.933+486C= (ZDHHC24)
NM_024649.5:c.952-55G= (BBS1) MANE Select NP_078925.3:n.952-55G=
NM_001348571.2:c.*22-2203C= (ZDHHC24) NP_001335500.1:n.*22-2203C=