Canonical Allele Identifier: CA2838894343

Gene: BBS9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33384077G>A , CM000669.2:g.33384077G>A	GRCh38
NC_000007.13:g.33423689G>A , CM000669.1:g.33423689G>A	GRCh37
NC_000007.12:g.33390214G>A	NCBI36
NG_009306.1:g.259538G>A
NG_009306.2:g.259834G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242067.11:c.1962+239G>A MANE Select	ENSP00000242067.6:n.1962+239G>A
ENST00000671871.1:c.2085+239G>A	ENSP00000499908.1:n.2085+239G>A
ENST00000671890.1:c.1827+239G>A	ENSP00000500146.1:n.1827+239G>A
ENST00000671952.1:c.1962+239G>A	ENSP00000500239.1:n.1962+239G>A
ENST00000671963.1:c.1596+239G>A	ENSP00000499904.1:n.1596+239G>A
ENST00000672453.1:n.1731+239G>A
ENST00000672717.1:c.1857+239G>A	ENSP00000499835.1:n.1857+239G>A
ENST00000672973.1:c.1962+239G>A	ENSP00000500017.1:n.1962+239G>A
ENST00000673056.1:c.1962+239G>A	ENSP00000499989.1:n.1962+239G>A
ENST00000673219.1:c.*1699+239G>A	ENSP00000499968.1:n.*1699+239G>A
ENST00000673230.1:n.1993+239G>A
ENST00000673431.1:c.1827+239G>A	ENSP00000500552.1:n.1827+239G>A
ENST00000673462.1:c.*708+239G>A	ENSP00000499848.1:n.*708+239G>A
ENST00000242067.10:c.1962+239G>A	ENSP00000242067.6:n.1962+239G>A
ENST00000350941.7:c.1842+239G>A	ENSP00000313122.6:n.1842+239G>A
ENST00000355070.6:c.1947+239G>A	ENSP00000347182.2:n.1947+239G>A
ENST00000396127.6:c.1857+239G>A	ENSP00000379433.2:n.1857+239G>A
ENST00000433714.5:c.*723+239G>A	ENSP00000412159.1:n.*723+239G>A
ENST00000434373.3:c.661+239G>A
ENST00000496029.1:n.85+239G>A
ENST00000627264.1:c.533+239G>A
NM_001033604.1:c.1857+239G>A	NP_001028776.1:n.1857+239G>A
NM_001033605.1:c.1947+239G>A	NP_001028777.1:n.1947+239G>A
NM_014451.3:c.1842+239G>A	NP_055266.2:n.1842+239G>A
NM_198428.2:c.1962+239G>A	NP_940820.1:n.1962+239G>A
XM_005249700.3:c.1962+239G>A	XP_005249757.1:n.1962+239G>A
XM_005249701.1:c.1962+239G>A	XP_005249758.1:n.1962+239G>A
XM_011515264.1:c.1962+239G>A	XP_011513566.1:n.1962+239G>A
XM_011515265.1:c.1962+239G>A	XP_011513567.1:n.1962+239G>A
XM_011515266.1:c.1947+239G>A	XP_011513568.1:n.1947+239G>A
XM_011515267.1:c.1857+239G>A	XP_011513569.1:n.1857+239G>A
XM_011515268.1:c.1962+239G>A	XP_011513570.1:n.1962+239G>A
XM_011515269.1:c.1689+239G>A	XP_011513571.1:n.1689+239G>A
XM_011515270.1:c.1962+239G>A	XP_011513572.1:n.1962+239G>A
NM_001348036.1:c.1962+239G>A	NP_001334965.1:n.1962+239G>A
NM_001348037.2:c.1596+239G>A	NP_001334966.1:n.1596+239G>A
NM_001348038.2:c.1689+239G>A	NP_001334967.1:n.1689+239G>A
NM_001348039.2:c.1584+239G>A	NP_001334968.1:n.1584+239G>A
NM_001348040.2:c.1842+239G>A	NP_001334969.1:n.1842+239G>A
NM_001348041.3:c.1962+239G>A	NP_001334970.1:n.1962+239G>A
NM_001348042.2:c.1827+239G>A	NP_001334971.1:n.1827+239G>A
NM_001348043.2:c.1962+239G>A	NP_001334972.1:n.1962+239G>A
NM_001348044.2:c.1491+239G>A	NP_001334973.1:n.1491+239G>A
NM_001348045.2:c.1596+239G>A	NP_001334974.1:n.1596+239G>A
NM_001348046.2:c.1596+239G>A	NP_001334975.1:n.1596+239G>A
NM_001362679.1:c.1962+239G>A	NP_001349608.1:n.1962+239G>A
NR_145411.1:n.2241+239G>A
NR_145412.1:n.2433+239G>A
NR_145413.2:n.2619+239G>A
XM_005249701.3:c.1962+239G>A	XP_005249758.1:n.1962+239G>A
XM_011515265.2:c.1962+239G>A	XP_011513567.1:n.1962+239G>A
XM_011515266.3:c.1947+239G>A	XP_011513568.1:n.1947+239G>A
XM_011515267.3:c.1857+239G>A	XP_011513569.1:n.1857+239G>A
XM_011515269.2:c.1689+239G>A	XP_011513571.1:n.1689+239G>A
XM_011515270.3:c.1962+239G>A	XP_011513572.1:n.1962+239G>A
XM_017011990.1:c.1947+239G>A	XP_016867479.1:n.1947+239G>A
NM_001348040.3:c.1842+239G>A	NP_001334969.1:n.1842+239G>A
NM_001348041.4:c.1962+239G>A	NP_001334970.1:n.1962+239G>A
NM_001348043.3:c.1962+239G>A	NP_001334972.1:n.1962+239G>A
NM_198428.3:c.1962+239G>A MANE Select	NP_940820.1:n.1962+239G>A
NM_001033604.2:c.1857+239G>A	NP_001028776.1:n.1857+239G>A
NM_001033605.2:c.1947+239G>A	NP_001028777.1:n.1947+239G>A
NM_001348037.3:c.1596+239G>A	NP_001334966.1:n.1596+239G>A
NM_001348038.3:c.1689+239G>A	NP_001334967.1:n.1689+239G>A
NM_001348039.3:c.1584+239G>A	NP_001334968.1:n.1584+239G>A
NM_001348042.3:c.1827+239G>A	NP_001334971.1:n.1827+239G>A
NM_001348044.3:c.1491+239G>A	NP_001334973.1:n.1491+239G>A
NM_001348045.3:c.1596+239G>A	NP_001334974.1:n.1596+239G>A
NM_001348046.3:c.1596+239G>A	NP_001334975.1:n.1596+239G>A
NM_014451.4:c.1842+239G>A	NP_055266.2:n.1842+239G>A
NR_145413.3:n.2595+239G>A