Canonical Allele Identifier: CA1979709902
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523676C= , CM000673.2:g.66523676C= GRCh38
NC_000011.9:g.66291147C= , CM000673.1:g.66291147C= GRCh37
NC_000011.8:g.66047723C= NCBI36
NG_009093.1:g.18029C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.952-48C= (BBS1) MANE Select ENSP00000317469.7:n.952-48C=
ENST00000318312.11:c.952-48C= (BBS1) ENSP00000317469.7:n.952-48C=
ENST00000393994.4:c.724-2447C= (BBS1) ENSP00000377563.2:n.724-2447C=
ENST00000419755.3:c.1063-48C= ENSP00000398526.3:n.1063-48C=
ENST00000455748.6:c.661-48C= (BBS1) ENSP00000405764.2:n.661-48C=
ENST00000526760.5:c.*659-48C= (BBS1) ENSP00000432140.1:n.*659-48C=
ENST00000526986.5:c.*22-2210G= (ZDHHC24) ENSP00000431321.1:n.*22-2210G=
ENST00000527959.1:n.96-48C= (BBS1)
ENST00000529766.5:n.959-48C= (BBS1)
ENST00000529895.1:n.401-48C= (BBS1)
ENST00000529955.5:n.923-48C= (BBS1)
ENST00000532908.5:c.*612-48C= (BBS1) ENSP00000431866.1:n.*612-48C=
ENST00000534073.5:c.*143+479G= (ZDHHC24) ENSP00000436503.1:n.*143+479G=
ENST00000630659.2:c.*659-48C= (BBS1) ENSP00000486455.1:n.*659-48C=
NM_024649.4:c.952-48C= (BBS1) NP_078925.3:n.952-48C=
XM_005273874.3:c.*22-2210G= (ZDHHC24) XP_005273931.1:n.*22-2210G=
XR_949860.1:n.808+479G= (ZDHHC24)
NM_001348571.1:c.*22-2210G= (ZDHHC24) NP_001335500.1:n.*22-2210G=
XM_005273874.4:c.*22-2210G= (ZDHHC24) XP_005273931.1:n.*22-2210G=
XR_001747823.2:n.862+479G= (ZDHHC24)
XR_949860.3:n.933+479G= (ZDHHC24)
NM_024649.5:c.952-48C= (BBS1) MANE Select NP_078925.3:n.952-48C=
NM_001348571.2:c.*22-2210G= (ZDHHC24) NP_001335500.1:n.*22-2210G=