Canonical Allele Identifier: CA2614500840
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523671T>A , CM000673.2:g.66523671T>A GRCh38
NC_000011.9:g.66291142T>A , CM000673.1:g.66291142T>A GRCh37
NC_000011.8:g.66047718T>A NCBI36
NG_009093.1:g.18024T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.952-53T>A (BBS1) MANE Select ENSP00000317469.7:n.952-53T>A
ENST00000318312.11:c.952-53T>A (BBS1) ENSP00000317469.7:n.952-53T>A
ENST00000393994.4:c.724-2452T>A (BBS1) ENSP00000377563.2:n.724-2452T>A
ENST00000419755.3:c.1063-53T>A ENSP00000398526.3:n.1063-53T>A
ENST00000455748.6:c.661-53T>A (BBS1) ENSP00000405764.2:n.661-53T>A
ENST00000526760.5:c.*659-53T>A (BBS1) ENSP00000432140.1:n.*659-53T>A
ENST00000526986.5:c.*22-2205A>T (ZDHHC24) ENSP00000431321.1:n.*22-2205A>T
ENST00000527959.1:n.96-53T>A (BBS1)
ENST00000529766.5:n.959-53T>A (BBS1)
ENST00000529895.1:n.401-53T>A (BBS1)
ENST00000529955.5:n.923-53T>A (BBS1)
ENST00000532908.5:c.*612-53T>A (BBS1) ENSP00000431866.1:n.*612-53T>A
ENST00000534073.5:c.*143+484A>T (ZDHHC24) ENSP00000436503.1:n.*143+484A>T
ENST00000630659.2:c.*659-53T>A (BBS1) ENSP00000486455.1:n.*659-53T>A
NM_024649.4:c.952-53T>A (BBS1) NP_078925.3:n.952-53T>A
XM_005273874.3:c.*22-2205A>T (ZDHHC24) XP_005273931.1:n.*22-2205A>T
XR_949860.1:n.808+484A>T (ZDHHC24)
NM_001348571.1:c.*22-2205A>T (ZDHHC24) NP_001335500.1:n.*22-2205A>T
XM_005273874.4:c.*22-2205A>T (ZDHHC24) XP_005273931.1:n.*22-2205A>T
XR_001747823.2:n.862+484A>T (ZDHHC24)
XR_949860.3:n.933+484A>T (ZDHHC24)
NM_024649.5:c.952-53T>A (BBS1) MANE Select NP_078925.3:n.952-53T>A
NM_001348571.2:c.*22-2205A>T (ZDHHC24) NP_001335500.1:n.*22-2205A>T