Canonical Allele Identifier: CA1979709972

Gene: BBS1 ZDHHC24

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523793C= , CM000673.2:g.66523793C=	GRCh38
NC_000011.9:g.66291264C= , CM000673.1:g.66291264C=	GRCh37
NC_000011.8:g.66047840C=	NCBI36
NG_009093.1:g.18146C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1021C= (BBS1) MANE Select	ENSP00000317469.7:p.Arg341=
ENST00000318312.11:c.1021C= (BBS1)	ENSP00000317469.7:p.Arg341=
ENST00000393994.4:c.724-2330C= (BBS1)	ENSP00000377563.2:n.724-2330C=
ENST00000419755.3:c.1132C=	ENSP00000398526.3:p.Arg378=
ENST00000455748.6:c.730C= (BBS1)	ENSP00000405764.2:p.Arg244=
ENST00000526760.5:c.*728C= (BBS1)	ENSP00000432140.1:n.*728C=
ENST00000526986.5:c.*22-2327G= (ZDHHC24)	ENSP00000431321.1:n.*22-2327G=
ENST00000527959.1:n.165C= (BBS1)
ENST00000529766.5:n.1028C= (BBS1)
ENST00000529895.1:n.470C= (BBS1)
ENST00000529955.5:n.992C= (BBS1)
ENST00000532908.5:c.*681C= (BBS1)	ENSP00000431866.1:n.*681C=
ENST00000534073.5:c.*143+362G= (ZDHHC24)	ENSP00000436503.1:n.*143+362G=
ENST00000630659.2:c.*728C= (BBS1)	ENSP00000486455.1:n.*728C=
NM_024649.4:c.1021C= (BBS1)	NP_078925.3:p.Arg341=
XM_005273874.3:c.*22-2327G= (ZDHHC24)	XP_005273931.1:n.*22-2327G=
XR_949860.1:n.808+362G= (ZDHHC24)
NM_001348571.1:c.*22-2327G= (ZDHHC24)	NP_001335500.1:n.*22-2327G=
XM_005273874.4:c.*22-2327G= (ZDHHC24)	XP_005273931.1:n.*22-2327G=
XR_001747823.2:n.862+362G= (ZDHHC24)
XR_949860.3:n.933+362G= (ZDHHC24)
NM_024649.5:c.1021C= (BBS1) MANE Select	NP_078925.3:p.Arg341=
NM_001348571.2:c.*22-2327G= (ZDHHC24)	NP_001335500.1:n.*22-2327G=