Canonical Allele Identifier: CA381462669
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523854A>G , CM000673.2:g.66523854A>G GRCh38
NC_000011.9:g.66291325A>G , CM000673.1:g.66291325A>G GRCh37
NC_000011.8:g.66047901A>G NCBI36
NG_009093.1:g.18207A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1082A>G (BBS1) MANE Select ENSP00000317469.7:p.Lys361Arg
ENST00000318312.11:c.1082A>G (BBS1) ENSP00000317469.7:p.Lys361Arg
ENST00000393994.4:c.724-2269A>G (BBS1) ENSP00000377563.2:n.724-2269A>G
ENST00000419755.3:c.1193A>G ENSP00000398526.3:p.Lys398Arg
ENST00000455748.6:c.791A>G (BBS1) ENSP00000405764.2:p.Lys264Arg
ENST00000526760.5:c.*789A>G (BBS1) ENSP00000432140.1:n.*789A>G
ENST00000526986.5:c.*22-2388T>C (ZDHHC24) ENSP00000431321.1:n.*22-2388T>C
ENST00000527959.1:n.226A>G (BBS1)
ENST00000529766.5:n.1089A>G (BBS1)
ENST00000529895.1:n.531A>G (BBS1)
ENST00000529955.5:n.1053A>G (BBS1)
ENST00000534073.5:c.*143+301T>C (ZDHHC24) ENSP00000436503.1:n.*143+301T>C
ENST00000630659.2:c.*789A>G (BBS1) ENSP00000486455.1:n.*789A>G
NM_024649.4:c.1082A>G (BBS1) NP_078925.3:p.Lys361Arg
XM_005273874.3:c.*22-2388T>C (ZDHHC24) XP_005273931.1:n.*22-2388T>C
XR_949860.1:n.808+301T>C (ZDHHC24)
NM_001348571.1:c.*22-2388T>C (ZDHHC24) NP_001335500.1:n.*22-2388T>C
XM_005273874.4:c.*22-2388T>C (ZDHHC24) XP_005273931.1:n.*22-2388T>C
XR_001747823.2:n.862+301T>C (ZDHHC24)
XR_949860.3:n.933+301T>C (ZDHHC24)
NM_024649.5:c.1082A>G (BBS1) MANE Select NP_078925.3:p.Lys361Arg
NM_001348571.2:c.*22-2388T>C (ZDHHC24) NP_001335500.1:n.*22-2388T>C