Canonical Allele Identifier: CA381422456
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1421044140

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526666A>G , CM000673.2:g.66526666A>G GRCh38
NC_000011.9:g.66294137A>G , CM000673.1:g.66294137A>G GRCh37
NC_000011.8:g.66050713A>G NCBI36
NG_009093.1:g.21019A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1198A>G (BBS1) MANE Select ENSP00000317469.7:p.Lys400Glu
ENST00000318312.11:c.1198A>G (BBS1) ENSP00000317469.7:p.Lys400Glu
ENST00000393994.4:c.811A>G (BBS1) ENSP00000377563.2:p.Lys271Glu
ENST00000419755.3:c.1309A>G ENSP00000398526.3:p.Lys437Glu
ENST00000455748.6:c.907A>G (BBS1) ENSP00000405764.2:p.Lys303Glu
ENST00000526760.5:c.*905A>G (BBS1) ENSP00000432140.1:n.*905A>G
ENST00000526986.5:c.*21+270T>C (ZDHHC24) ENSP00000431321.1:n.*21+270T>C
ENST00000527959.1:n.342A>G (BBS1)
ENST00000529766.5:n.1205A>G (BBS1)
ENST00000529955.5:n.1169A>G (BBS1)
ENST00000534073.5:c.*21+270T>C (ZDHHC24) ENSP00000436503.1:n.*21+270T>C
ENST00000630659.2:c.*905A>G (BBS1) ENSP00000486455.1:n.*905A>G
NM_024649.4:c.1198A>G (BBS1) NP_078925.3:p.Lys400Glu
XM_005273874.3:c.*21+270T>C (ZDHHC24) XP_005273931.1:n.*21+270T>C
XM_011544894.1:c.*21+270T>C (ZDHHC24) XP_011543196.1:n.*21+270T>C
XM_011544895.1:c.560-2390T>C (ZDHHC24) XP_011543197.1:n.560-2390T>C
XR_949860.1:n.686+270T>C (ZDHHC24)
NM_001348571.1:c.*21+270T>C (ZDHHC24) NP_001335500.1:n.*21+270T>C
XM_005273874.4:c.*21+270T>C (ZDHHC24) XP_005273931.1:n.*21+270T>C
XM_011544894.2:c.*21+270T>C (ZDHHC24) XP_011543196.1:n.*21+270T>C
XR_001747823.2:n.741-2390T>C (ZDHHC24)
XR_949860.3:n.811+270T>C (ZDHHC24)
NM_024649.5:c.1198A>G (BBS1) MANE Select NP_078925.3:p.Lys400Glu
NM_001348571.2:c.*21+270T>C (ZDHHC24) NP_001335500.1:n.*21+270T>C