Canonical Allele Identifier: CA381462622
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523845A>C , CM000673.2:g.66523845A>C GRCh38
NC_000011.9:g.66291316A>C , CM000673.1:g.66291316A>C GRCh37
NC_000011.8:g.66047892A>C NCBI36
NG_009093.1:g.18198A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1073A>C (BBS1) MANE Select ENSP00000317469.7:p.Tyr358Ser
ENST00000318312.11:c.1073A>C (BBS1) ENSP00000317469.7:p.Tyr358Ser
ENST00000393994.4:c.724-2278A>C (BBS1) ENSP00000377563.2:n.724-2278A>C
ENST00000419755.3:c.1184A>C ENSP00000398526.3:p.Tyr395Ser
ENST00000455748.6:c.782A>C (BBS1) ENSP00000405764.2:p.Tyr261Ser
ENST00000526760.5:c.*780A>C (BBS1) ENSP00000432140.1:n.*780A>C
ENST00000526986.5:c.*22-2379T>G (ZDHHC24) ENSP00000431321.1:n.*22-2379T>G
ENST00000527959.1:n.217A>C (BBS1)
ENST00000529766.5:n.1080A>C (BBS1)
ENST00000529895.1:n.522A>C (BBS1)
ENST00000529955.5:n.1044A>C (BBS1)
ENST00000534073.5:c.*143+310T>G (ZDHHC24) ENSP00000436503.1:n.*143+310T>G
ENST00000630659.2:c.*780A>C (BBS1) ENSP00000486455.1:n.*780A>C
NM_024649.4:c.1073A>C (BBS1) NP_078925.3:p.Tyr358Ser
XM_005273874.3:c.*22-2379T>G (ZDHHC24) XP_005273931.1:n.*22-2379T>G
XR_949860.1:n.808+310T>G (ZDHHC24)
NM_001348571.1:c.*22-2379T>G (ZDHHC24) NP_001335500.1:n.*22-2379T>G
XM_005273874.4:c.*22-2379T>G (ZDHHC24) XP_005273931.1:n.*22-2379T>G
XR_001747823.2:n.862+310T>G (ZDHHC24)
XR_949860.3:n.933+310T>G (ZDHHC24)
NM_024649.5:c.1073A>C (BBS1) MANE Select NP_078925.3:p.Tyr358Ser
NM_001348571.2:c.*22-2379T>G (ZDHHC24) NP_001335500.1:n.*22-2379T>G