Canonical Allele Identifier: CA381462651
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523850G>C , CM000673.2:g.66523850G>C GRCh38
NC_000011.9:g.66291321G>C , CM000673.1:g.66291321G>C GRCh37
NC_000011.8:g.66047897G>C NCBI36
NG_009093.1:g.18203G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1078G>C (BBS1) MANE Select ENSP00000317469.7:p.Asp360His
ENST00000318312.11:c.1078G>C (BBS1) ENSP00000317469.7:p.Asp360His
ENST00000393994.4:c.724-2273G>C (BBS1) ENSP00000377563.2:n.724-2273G>C
ENST00000419755.3:c.1189G>C ENSP00000398526.3:p.Asp397His
ENST00000455748.6:c.787G>C (BBS1) ENSP00000405764.2:p.Asp263His
ENST00000526760.5:c.*785G>C (BBS1) ENSP00000432140.1:n.*785G>C
ENST00000526986.5:c.*22-2384C>G (ZDHHC24) ENSP00000431321.1:n.*22-2384C>G
ENST00000527959.1:n.222G>C (BBS1)
ENST00000529766.5:n.1085G>C (BBS1)
ENST00000529895.1:n.527G>C (BBS1)
ENST00000529955.5:n.1049G>C (BBS1)
ENST00000534073.5:c.*143+305C>G (ZDHHC24) ENSP00000436503.1:n.*143+305C>G
ENST00000630659.2:c.*785G>C (BBS1) ENSP00000486455.1:n.*785G>C
NM_024649.4:c.1078G>C (BBS1) NP_078925.3:p.Asp360His
XM_005273874.3:c.*22-2384C>G (ZDHHC24) XP_005273931.1:n.*22-2384C>G
XR_949860.1:n.808+305C>G (ZDHHC24)
NM_001348571.1:c.*22-2384C>G (ZDHHC24) NP_001335500.1:n.*22-2384C>G
XM_005273874.4:c.*22-2384C>G (ZDHHC24) XP_005273931.1:n.*22-2384C>G
XR_001747823.2:n.862+305C>G (ZDHHC24)
XR_949860.3:n.933+305C>G (ZDHHC24)
NM_024649.5:c.1078G>C (BBS1) MANE Select NP_078925.3:p.Asp360His
NM_001348571.2:c.*22-2384C>G (ZDHHC24) NP_001335500.1:n.*22-2384C>G