Canonical Allele Identifier: CA6123570
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

dbSNP Id: rs778802597

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523695C>T , CM000673.2:g.66523695C>T GRCh38
NC_000011.9:g.66291166C>T , CM000673.1:g.66291166C>T GRCh37
NC_000011.8:g.66047742C>T NCBI36
NG_009093.1:g.18048C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.952-29C>T (BBS1) MANE Select ENSP00000317469.7:n.952-29C>T
ENST00000318312.11:c.952-29C>T (BBS1) ENSP00000317469.7:n.952-29C>T
ENST00000393994.4:c.724-2428C>T (BBS1) ENSP00000377563.2:n.724-2428C>T
ENST00000419755.3:c.1063-29C>T ENSP00000398526.3:n.1063-29C>T
ENST00000455748.6:c.661-29C>T (BBS1) ENSP00000405764.2:n.661-29C>T
ENST00000526760.5:c.*659-29C>T (BBS1) ENSP00000432140.1:n.*659-29C>T
ENST00000526986.5:c.*22-2229G>A (ZDHHC24) ENSP00000431321.1:n.*22-2229G>A
ENST00000527959.1:n.96-29C>T (BBS1)
ENST00000529766.5:n.959-29C>T (BBS1)
ENST00000529895.1:n.401-29C>T (BBS1)
ENST00000529955.5:n.923-29C>T (BBS1)
ENST00000532908.5:c.*612-29C>T (BBS1) ENSP00000431866.1:n.*612-29C>T
ENST00000534073.5:c.*143+460G>A (ZDHHC24) ENSP00000436503.1:n.*143+460G>A
ENST00000630659.2:c.*659-29C>T (BBS1) ENSP00000486455.1:n.*659-29C>T
NM_024649.4:c.952-29C>T (BBS1) NP_078925.3:n.952-29C>T
XM_005273874.3:c.*22-2229G>A (ZDHHC24) XP_005273931.1:n.*22-2229G>A
XR_949860.1:n.808+460G>A (ZDHHC24)
NM_001348571.1:c.*22-2229G>A (ZDHHC24) NP_001335500.1:n.*22-2229G>A
XM_005273874.4:c.*22-2229G>A (ZDHHC24) XP_005273931.1:n.*22-2229G>A
XR_001747823.2:n.862+460G>A (ZDHHC24)
XR_949860.3:n.933+460G>A (ZDHHC24)
NM_024649.5:c.952-29C>T (BBS1) MANE Select NP_078925.3:n.952-29C>T
NM_001348571.2:c.*22-2229G>A (ZDHHC24) NP_001335500.1:n.*22-2229G>A