Canonical Allele Identifier: CA1698730800
Gene: BBS9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33367711A= , CM000669.2:g.33367711A= GRCh38
NC_000007.13:g.33407323A= , CM000669.1:g.33407323A= GRCh37
NC_000007.12:g.33373848A= NCBI36
NG_009306.1:g.243172A=
NG_009306.2:g.243468A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242067.11:c.1694-56A= MANE Select ENSP00000242067.6:n.1694-56A=
ENST00000671871.1:c.1817-56A= ENSP00000499908.1:n.1817-56A=
ENST00000671890.1:c.1559-56A= ENSP00000500146.1:n.1559-56A=
ENST00000671952.1:c.1694-56A= ENSP00000500239.1:n.1694-56A=
ENST00000671963.1:c.1328-56A= ENSP00000499904.1:n.1328-56A=
ENST00000672453.1:n.1463-56A=
ENST00000672717.1:c.1589-56A= ENSP00000499835.1:n.1589-56A=
ENST00000672973.1:c.1694-56A= ENSP00000500017.1:n.1694-56A=
ENST00000673056.1:c.1694-56A= ENSP00000499989.1:n.1694-56A=
ENST00000673219.1:c.*1431-56A= ENSP00000499968.1:n.*1431-56A=
ENST00000673230.1:n.1725-56A=
ENST00000673431.1:c.1559-56A= ENSP00000500552.1:n.1559-56A=
ENST00000673462.1:c.*440-56A= ENSP00000499848.1:n.*440-56A=
ENST00000242067.10:c.1694-56A= ENSP00000242067.6:n.1694-56A=
ENST00000350941.7:c.1574-56A= ENSP00000313122.6:n.1574-56A=
ENST00000355070.6:c.1679-56A= ENSP00000347182.2:n.1679-56A=
ENST00000396127.6:c.1589-56A= ENSP00000379433.2:n.1589-56A=
ENST00000433714.5:c.*455-56A= ENSP00000412159.1:n.*455-56A=
ENST00000434373.3:c.393-56A=
ENST00000627264.1:c.265-56A=
NM_001033604.1:c.1589-56A= NP_001028776.1:n.1589-56A=
NM_001033605.1:c.1679-56A= NP_001028777.1:n.1679-56A=
NM_014451.3:c.1574-56A= NP_055266.2:n.1574-56A=
NM_198428.2:c.1694-56A= NP_940820.1:n.1694-56A=
XM_005249700.3:c.1694-56A= XP_005249757.1:n.1694-56A=
XM_005249701.1:c.1694-56A= XP_005249758.1:n.1694-56A=
XM_011515264.1:c.1694-56A= XP_011513566.1:n.1694-56A=
XM_011515265.1:c.1694-56A= XP_011513567.1:n.1694-56A=
XM_011515266.1:c.1679-56A= XP_011513568.1:n.1679-56A=
XM_011515267.1:c.1589-56A= XP_011513569.1:n.1589-56A=
XM_011515268.1:c.1694-56A= XP_011513570.1:n.1694-56A=
XM_011515269.1:c.1421-56A= XP_011513571.1:n.1421-56A=
XM_011515270.1:c.1694-56A= XP_011513572.1:n.1694-56A=
NM_001348036.1:c.1694-56A= NP_001334965.1:n.1694-56A=
NM_001348037.2:c.1328-56A= NP_001334966.1:n.1328-56A=
NM_001348038.2:c.1421-56A= NP_001334967.1:n.1421-56A=
NM_001348039.2:c.1316-56A= NP_001334968.1:n.1316-56A=
NM_001348040.2:c.1574-56A= NP_001334969.1:n.1574-56A=
NM_001348041.3:c.1694-56A= NP_001334970.1:n.1694-56A=
NM_001348042.2:c.1559-56A= NP_001334971.1:n.1559-56A=
NM_001348043.2:c.1694-56A= NP_001334972.1:n.1694-56A=
NM_001348044.2:c.1223-56A= NP_001334973.1:n.1223-56A=
NM_001348045.2:c.1328-56A= NP_001334974.1:n.1328-56A=
NM_001348046.2:c.1328-56A= NP_001334975.1:n.1328-56A=
NM_001362679.1:c.1694-56A= NP_001349608.1:n.1694-56A=
NR_145411.1:n.1973-56A=
NR_145412.1:n.2165-56A=
NR_145413.2:n.2351-56A=
XM_005249701.3:c.1694-56A= XP_005249758.1:n.1694-56A=
XM_011515265.2:c.1694-56A= XP_011513567.1:n.1694-56A=
XM_011515266.3:c.1679-56A= XP_011513568.1:n.1679-56A=
XM_011515267.3:c.1589-56A= XP_011513569.1:n.1589-56A=
XM_011515269.2:c.1421-56A= XP_011513571.1:n.1421-56A=
XM_011515270.3:c.1694-56A= XP_011513572.1:n.1694-56A=
XM_017011990.1:c.1679-56A= XP_016867479.1:n.1679-56A=
XM_017011994.2:c.*48-56A= XP_016867483.1:n.*48-56A=
NM_001348040.3:c.1574-56A= NP_001334969.1:n.1574-56A=
NM_001348041.4:c.1694-56A= NP_001334970.1:n.1694-56A=
NM_001348043.3:c.1694-56A= NP_001334972.1:n.1694-56A=
NM_198428.3:c.1694-56A= MANE Select NP_940820.1:n.1694-56A=
NM_001033604.2:c.1589-56A= NP_001028776.1:n.1589-56A=
NM_001033605.2:c.1679-56A= NP_001028777.1:n.1679-56A=
NM_001348037.3:c.1328-56A= NP_001334966.1:n.1328-56A=
NM_001348038.3:c.1421-56A= NP_001334967.1:n.1421-56A=
NM_001348039.3:c.1316-56A= NP_001334968.1:n.1316-56A=
NM_001348042.3:c.1559-56A= NP_001334971.1:n.1559-56A=
NM_001348044.3:c.1223-56A= NP_001334973.1:n.1223-56A=
NM_001348045.3:c.1328-56A= NP_001334974.1:n.1328-56A=
NM_001348046.3:c.1328-56A= NP_001334975.1:n.1328-56A=
NM_014451.4:c.1574-56A= NP_055266.2:n.1574-56A=
NR_145413.3:n.2327-56A=