Canonical Allele Identifier: CA2614500822
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523632G>A , CM000673.2:g.66523632G>A GRCh38
NC_000011.9:g.66291103G>A , CM000673.1:g.66291103G>A GRCh37
NC_000011.8:g.66047679G>A NCBI36
NG_009093.1:g.17985G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.951+56G>A (BBS1) MANE Select ENSP00000317469.7:n.951+56G>A
ENST00000318312.11:c.951+56G>A (BBS1) ENSP00000317469.7:n.951+56G>A
ENST00000393994.4:c.724-2491G>A (BBS1) ENSP00000377563.2:n.724-2491G>A
ENST00000419755.3:c.1062+56G>A ENSP00000398526.3:n.1062+56G>A
ENST00000455748.6:c.660+56G>A (BBS1) ENSP00000405764.2:n.660+56G>A
ENST00000526760.5:c.*658+56G>A (BBS1) ENSP00000432140.1:n.*658+56G>A
ENST00000526986.5:c.*22-2166C>T (ZDHHC24) ENSP00000431321.1:n.*22-2166C>T
ENST00000527959.1:n.95+56G>A (BBS1)
ENST00000529766.5:n.958+56G>A (BBS1)
ENST00000529895.1:n.400+56G>A (BBS1)
ENST00000529955.5:n.922+56G>A (BBS1)
ENST00000532908.5:c.*611+56G>A (BBS1) ENSP00000431866.1:n.*611+56G>A
ENST00000534073.5:c.*143+523C>T (ZDHHC24) ENSP00000436503.1:n.*143+523C>T
ENST00000630659.2:c.*658+56G>A (BBS1) ENSP00000486455.1:n.*658+56G>A
NM_024649.4:c.951+56G>A (BBS1) NP_078925.3:n.951+56G>A
XM_005273874.3:c.*22-2166C>T (ZDHHC24) XP_005273931.1:n.*22-2166C>T
XR_949860.1:n.808+523C>T (ZDHHC24)
NM_001348571.1:c.*22-2166C>T (ZDHHC24) NP_001335500.1:n.*22-2166C>T
XM_005273874.4:c.*22-2166C>T (ZDHHC24) XP_005273931.1:n.*22-2166C>T
XR_001747823.2:n.862+523C>T (ZDHHC24)
XR_949860.3:n.933+523C>T (ZDHHC24)
NM_024649.5:c.951+56G>A (BBS1) MANE Select NP_078925.3:n.951+56G>A
NM_001348571.2:c.*22-2166C>T (ZDHHC24) NP_001335500.1:n.*22-2166C>T