Canonical Allele Identifier: CA1979711881
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526720C= , CM000673.2:g.66526720C= GRCh38
NC_000011.9:g.66294191C= , CM000673.1:g.66294191C= GRCh37
NC_000011.8:g.66050767C= NCBI36
NG_009093.1:g.21073C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1252C= (BBS1) MANE Select ENSP00000317469.7:p.Pro418=
ENST00000318312.11:c.1252C= (BBS1) ENSP00000317469.7:p.Pro418=
ENST00000393994.4:c.865C= (BBS1) ENSP00000377563.2:p.Pro289=
ENST00000419755.3:c.1363C= ENSP00000398526.3:p.Pro455=
ENST00000455748.6:c.961C= (BBS1) ENSP00000405764.2:p.Pro321=
ENST00000526760.5:c.*959C= (BBS1) ENSP00000432140.1:n.*959C=
ENST00000526986.5:c.*21+216G= (ZDHHC24) ENSP00000431321.1:n.*21+216G=
ENST00000527959.1:n.396C= (BBS1)
ENST00000529766.5:n.1259C= (BBS1)
ENST00000529955.5:n.1223C= (BBS1)
ENST00000534073.5:c.*21+216G= (ZDHHC24) ENSP00000436503.1:n.*21+216G=
ENST00000630659.2:c.*959C= (BBS1) ENSP00000486455.1:n.*959C=
NM_024649.4:c.1252C= (BBS1) NP_078925.3:p.Pro418=
XM_005273874.3:c.*21+216G= (ZDHHC24) XP_005273931.1:n.*21+216G=
XM_011544894.1:c.*21+216G= (ZDHHC24) XP_011543196.1:n.*21+216G=
XM_011544895.1:c.560-2444G= (ZDHHC24) XP_011543197.1:n.560-2444G=
XR_949860.1:n.686+216G= (ZDHHC24)
NM_001348571.1:c.*21+216G= (ZDHHC24) NP_001335500.1:n.*21+216G=
XM_005273874.4:c.*21+216G= (ZDHHC24) XP_005273931.1:n.*21+216G=
XM_011544894.2:c.*21+216G= (ZDHHC24) XP_011543196.1:n.*21+216G=
XR_001747823.2:n.741-2444G= (ZDHHC24)
XR_949860.3:n.811+216G= (ZDHHC24)
NM_024649.5:c.1252C= (BBS1) MANE Select NP_078925.3:p.Pro418=
NM_001348571.2:c.*21+216G= (ZDHHC24) NP_001335500.1:n.*21+216G=