Canonical Allele Identifier: CA381462633
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523846T>A , CM000673.2:g.66523846T>A GRCh38
NC_000011.9:g.66291317T>A , CM000673.1:g.66291317T>A GRCh37
NC_000011.8:g.66047893T>A NCBI36
NG_009093.1:g.18199T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1074T>A (BBS1) MANE Select ENSP00000317469.7:p.Tyr358Ter
ENST00000318312.11:c.1074T>A (BBS1) ENSP00000317469.7:p.Tyr358Ter
ENST00000393994.4:c.724-2277T>A (BBS1) ENSP00000377563.2:n.724-2277T>A
ENST00000419755.3:c.1185T>A ENSP00000398526.3:p.Tyr395Ter
ENST00000455748.6:c.783T>A (BBS1) ENSP00000405764.2:p.Tyr261Ter
ENST00000526760.5:c.*781T>A (BBS1) ENSP00000432140.1:n.*781T>A
ENST00000526986.5:c.*22-2380A>T (ZDHHC24) ENSP00000431321.1:n.*22-2380A>T
ENST00000527959.1:n.218T>A (BBS1)
ENST00000529766.5:n.1081T>A (BBS1)
ENST00000529895.1:n.523T>A (BBS1)
ENST00000529955.5:n.1045T>A (BBS1)
ENST00000534073.5:c.*143+309A>T (ZDHHC24) ENSP00000436503.1:n.*143+309A>T
ENST00000630659.2:c.*781T>A (BBS1) ENSP00000486455.1:n.*781T>A
NM_024649.4:c.1074T>A (BBS1) NP_078925.3:p.Tyr358Ter
XM_005273874.3:c.*22-2380A>T (ZDHHC24) XP_005273931.1:n.*22-2380A>T
XR_949860.1:n.808+309A>T (ZDHHC24)
NM_001348571.1:c.*22-2380A>T (ZDHHC24) NP_001335500.1:n.*22-2380A>T
XM_005273874.4:c.*22-2380A>T (ZDHHC24) XP_005273931.1:n.*22-2380A>T
XR_001747823.2:n.862+309A>T (ZDHHC24)
XR_949860.3:n.933+309A>T (ZDHHC24)
NM_024649.5:c.1074T>A (BBS1) MANE Select NP_078925.3:p.Tyr358Ter
NM_001348571.2:c.*22-2380A>T (ZDHHC24) NP_001335500.1:n.*22-2380A>T