Canonical Allele Identifier: CA381462686
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523856G>A , CM000673.2:g.66523856G>A GRCh38
NC_000011.9:g.66291327G>A , CM000673.1:g.66291327G>A GRCh37
NC_000011.8:g.66047903G>A NCBI36
NG_009093.1:g.18209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1084G>A (BBS1) MANE Select ENSP00000317469.7:p.Ala362Thr
ENST00000318312.11:c.1084G>A (BBS1) ENSP00000317469.7:p.Ala362Thr
ENST00000393994.4:c.724-2267G>A (BBS1) ENSP00000377563.2:n.724-2267G>A
ENST00000419755.3:c.1195G>A ENSP00000398526.3:p.Ala399Thr
ENST00000455748.6:c.793G>A (BBS1) ENSP00000405764.2:p.Ala265Thr
ENST00000526760.5:c.*791G>A (BBS1) ENSP00000432140.1:n.*791G>A
ENST00000526986.5:c.*22-2390C>T (ZDHHC24) ENSP00000431321.1:n.*22-2390C>T
ENST00000527959.1:n.228G>A (BBS1)
ENST00000529766.5:n.1091G>A (BBS1)
ENST00000529895.1:n.533G>A (BBS1)
ENST00000529955.5:n.1055G>A (BBS1)
ENST00000534073.5:c.*143+299C>T (ZDHHC24) ENSP00000436503.1:n.*143+299C>T
ENST00000630659.2:c.*791G>A (BBS1) ENSP00000486455.1:n.*791G>A
NM_024649.4:c.1084G>A (BBS1) NP_078925.3:p.Ala362Thr
XM_005273874.3:c.*22-2390C>T (ZDHHC24) XP_005273931.1:n.*22-2390C>T
XR_949860.1:n.808+299C>T (ZDHHC24)
NM_001348571.1:c.*22-2390C>T (ZDHHC24) NP_001335500.1:n.*22-2390C>T
XM_005273874.4:c.*22-2390C>T (ZDHHC24) XP_005273931.1:n.*22-2390C>T
XR_001747823.2:n.862+299C>T (ZDHHC24)
XR_949860.3:n.933+299C>T (ZDHHC24)
NM_024649.5:c.1084G>A (BBS1) MANE Select NP_078925.3:p.Ala362Thr
NM_001348571.2:c.*22-2390C>T (ZDHHC24) NP_001335500.1:n.*22-2390C>T