Canonical Allele Identifier: CA1979712040
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526847A= , CM000673.2:g.66526847A= GRCh38
NC_000011.9:g.66294318A= , CM000673.1:g.66294318A= GRCh37
NC_000011.8:g.66050894A= NCBI36
NG_009093.1:g.21200A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1339+40A= (BBS1) MANE Select ENSP00000317469.7:n.1339+40A=
ENST00000318312.11:c.1339+40A= (BBS1) ENSP00000317469.7:n.1339+40A=
ENST00000393994.4:c.952+40A= (BBS1) ENSP00000377563.2:n.952+40A=
ENST00000419755.3:c.1450+40A= ENSP00000398526.3:n.1450+40A=
ENST00000455748.6:c.1048+40A= (BBS1) ENSP00000405764.2:n.1048+40A=
ENST00000526760.5:c.*1046+40A= (BBS1) ENSP00000432140.1:n.*1046+40A=
ENST00000526986.5:c.*21+89T= (ZDHHC24) ENSP00000431321.1:n.*21+89T=
ENST00000527959.1:n.523A= (BBS1)
ENST00000529766.5:n.1386A= (BBS1)
ENST00000529955.5:n.1310+40A= (BBS1)
ENST00000534073.5:c.*21+89T= (ZDHHC24) ENSP00000436503.1:n.*21+89T=
ENST00000630659.2:c.*1046+40A= (BBS1) ENSP00000486455.1:n.*1046+40A=
NM_024649.4:c.1339+40A= (BBS1) NP_078925.3:n.1339+40A=
XM_005273874.3:c.*21+89T= (ZDHHC24) XP_005273931.1:n.*21+89T=
XM_011544894.1:c.*21+89T= (ZDHHC24) XP_011543196.1:n.*21+89T=
XM_011544895.1:c.560-2571T= (ZDHHC24) XP_011543197.1:n.560-2571T=
XR_949860.1:n.686+89T= (ZDHHC24)
NM_001348571.1:c.*21+89T= (ZDHHC24) NP_001335500.1:n.*21+89T=
XM_005273874.4:c.*21+89T= (ZDHHC24) XP_005273931.1:n.*21+89T=
XM_011544894.2:c.*21+89T= (ZDHHC24) XP_011543196.1:n.*21+89T=
XR_001747823.2:n.741-2571T= (ZDHHC24)
XR_949860.3:n.811+89T= (ZDHHC24)
NM_024649.5:c.1339+40A= (BBS1) MANE Select NP_078925.3:n.1339+40A=
NM_001348571.2:c.*21+89T= (ZDHHC24) NP_001335500.1:n.*21+89T=