Canonical Allele Identifier: CA381462163
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523761T>G , CM000673.2:g.66523761T>G GRCh38
NC_000011.9:g.66291232T>G , CM000673.1:g.66291232T>G GRCh37
NC_000011.8:g.66047808T>G NCBI36
NG_009093.1:g.18114T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.989T>G (BBS1) MANE Select ENSP00000317469.7:p.Ile330Ser
ENST00000318312.11:c.989T>G (BBS1) ENSP00000317469.7:p.Ile330Ser
ENST00000393994.4:c.724-2362T>G (BBS1) ENSP00000377563.2:n.724-2362T>G
ENST00000419755.3:c.1100T>G ENSP00000398526.3:p.Ile367Ser
ENST00000455748.6:c.698T>G (BBS1) ENSP00000405764.2:p.Ile233Ser
ENST00000526760.5:c.*696T>G (BBS1) ENSP00000432140.1:n.*696T>G
ENST00000526986.5:c.*22-2295A>C (ZDHHC24) ENSP00000431321.1:n.*22-2295A>C
ENST00000527959.1:n.133T>G (BBS1)
ENST00000529766.5:n.996T>G (BBS1)
ENST00000529895.1:n.438T>G (BBS1)
ENST00000529955.5:n.960T>G (BBS1)
ENST00000532908.5:c.*649T>G (BBS1) ENSP00000431866.1:n.*649T>G
ENST00000534073.5:c.*143+394A>C (ZDHHC24) ENSP00000436503.1:n.*143+394A>C
ENST00000630659.2:c.*696T>G (BBS1) ENSP00000486455.1:n.*696T>G
NM_024649.4:c.989T>G (BBS1) NP_078925.3:p.Ile330Ser
XM_005273874.3:c.*22-2295A>C (ZDHHC24) XP_005273931.1:n.*22-2295A>C
XR_949860.1:n.808+394A>C (ZDHHC24)
NM_001348571.1:c.*22-2295A>C (ZDHHC24) NP_001335500.1:n.*22-2295A>C
XM_005273874.4:c.*22-2295A>C (ZDHHC24) XP_005273931.1:n.*22-2295A>C
XR_001747823.2:n.862+394A>C (ZDHHC24)
XR_949860.3:n.933+394A>C (ZDHHC24)
NM_024649.5:c.989T>G (BBS1) MANE Select NP_078925.3:p.Ile330Ser
NM_001348571.2:c.*22-2295A>C (ZDHHC24) NP_001335500.1:n.*22-2295A>C