Canonical Allele Identifier: CA342396
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

ClinVar Variation Id: 21706
ClinVar RCV Id: RCV000020904
dbSNP Id: rs113994180

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66529817A>G , CM000673.2:g.66529817A>G GRCh38
NC_000011.9:g.66297288A>G , CM000673.1:g.66297288A>G GRCh37
NC_000011.8:g.66053864A>G NCBI36
NG_009093.1:g.24170A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.1340-2A>G (BBS1) MANE Select ENSP00000317469.7:n.1340-2A>G
ENST00000318312.11:c.1340-2A>G (BBS1) ENSP00000317469.7:n.1340-2A>G
ENST00000393994.4:c.953-2A>G (BBS1) ENSP00000377563.2:n.953-2A>G
ENST00000419755.3:c.1451-2A>G ENSP00000398526.3:n.1451-2A>G
ENST00000455748.6:c.1049-2A>G (BBS1) ENSP00000405764.2:n.1049-2A>G
ENST00000526760.5:c.*1047-2A>G (BBS1) ENSP00000432140.1:n.*1047-2A>G
ENST00000526986.5:c.560-329T>C (ZDHHC24) ENSP00000431321.1:n.560-329T>C
ENST00000529955.5:n.1311-2A>G (BBS1)
ENST00000534073.5:c.560-2811T>C (ZDHHC24) ENSP00000436503.1:n.560-2811T>C
ENST00000630659.2:c.*1047-2A>G (BBS1) ENSP00000486455.1:n.*1047-2A>G
NM_024649.4:c.1340-2A>G (BBS1) NP_078925.3:n.1340-2A>G
XM_005273874.3:c.560-2811T>C (ZDHHC24) XP_005273931.1:n.560-2811T>C
XM_011544891.1:c.560-329T>C (ZDHHC24) XP_011543193.1:n.560-329T>C
XM_011544894.1:c.560-2811T>C (ZDHHC24) XP_011543196.1:n.560-2811T>C
XM_011544895.1:c.560-5541T>C (ZDHHC24) XP_011543197.1:n.560-5541T>C
XR_949860.1:n.616-2811T>C (ZDHHC24)
NM_001348571.1:c.560-329T>C (ZDHHC24) NP_001335500.1:n.560-329T>C
XM_005273874.4:c.560-2811T>C (ZDHHC24) XP_005273931.1:n.560-2811T>C
XM_011544894.2:c.560-2811T>C (ZDHHC24) XP_011543196.1:n.560-2811T>C
XR_001747823.2:n.741-5541T>C (ZDHHC24)
XR_949860.3:n.741-2811T>C (ZDHHC24)
NM_024649.5:c.1340-2A>G (BBS1) MANE Select NP_078925.3:n.1340-2A>G
NM_001348571.2:c.560-329T>C (ZDHHC24) NP_001335500.1:n.560-329T>C