Canonical Allele Identifier: CA1979709942

Gene: BBS1 ZDHHC24

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523744G= , CM000673.2:g.66523744G=	GRCh38
NC_000011.9:g.66291215G= , CM000673.1:g.66291215G=	GRCh37
NC_000011.8:g.66047791G=	NCBI36
NG_009093.1:g.18097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.972G= (BBS1) MANE Select	ENSP00000317469.7:p.Val324=
ENST00000318312.11:c.972G= (BBS1)	ENSP00000317469.7:p.Val324=
ENST00000393994.4:c.724-2379G= (BBS1)	ENSP00000377563.2:n.724-2379G=
ENST00000419755.3:c.1083G=	ENSP00000398526.3:p.Val361=
ENST00000455748.6:c.681G= (BBS1)	ENSP00000405764.2:p.Val227=
ENST00000526760.5:c.*679G= (BBS1)	ENSP00000432140.1:n.*679G=
ENST00000526986.5:c.*22-2278C= (ZDHHC24)	ENSP00000431321.1:n.*22-2278C=
ENST00000527959.1:n.116G= (BBS1)
ENST00000529766.5:n.979G= (BBS1)
ENST00000529895.1:n.421G= (BBS1)
ENST00000529955.5:n.943G= (BBS1)
ENST00000532908.5:c.*632G= (BBS1)	ENSP00000431866.1:n.*632G=
ENST00000534073.5:c.*143+411C= (ZDHHC24)	ENSP00000436503.1:n.*143+411C=
ENST00000630659.2:c.*679G= (BBS1)	ENSP00000486455.1:n.*679G=
NM_024649.4:c.972G= (BBS1)	NP_078925.3:p.Val324=
XM_005273874.3:c.*22-2278C= (ZDHHC24)	XP_005273931.1:n.*22-2278C=
XR_949860.1:n.808+411C= (ZDHHC24)
NM_001348571.1:c.*22-2278C= (ZDHHC24)	NP_001335500.1:n.*22-2278C=
XM_005273874.4:c.*22-2278C= (ZDHHC24)	XP_005273931.1:n.*22-2278C=
XR_001747823.2:n.862+411C= (ZDHHC24)
XR_949860.3:n.933+411C= (ZDHHC24)
NM_024649.5:c.972G= (BBS1) MANE Select	NP_078925.3:p.Val324=
NM_001348571.2:c.*22-2278C= (ZDHHC24)	NP_001335500.1:n.*22-2278C=