Canonical Allele Identifier: CA475337286

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66294205C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66526734C>A , CM000673.2:g.66526734C>A	GRCh38
NC_000011.9:g.66294205C>A , CM000673.1:g.66294205C>A	GRCh37
NC_000011.8:g.66050781C>A	NCBI36
NG_009093.1:g.21087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1266C>A (BBS1) MANE Select	ENSP00000317469.7:p.Ala422=
ENST00000318312.11:c.1266C>A (BBS1)	ENSP00000317469.7:p.Ala422=
ENST00000393994.4:c.879C>A (BBS1)	ENSP00000377563.2:p.Ala293=
ENST00000419755.3:c.1377C>A	ENSP00000398526.3:p.Ala459=
ENST00000455748.6:c.975C>A (BBS1)	ENSP00000405764.2:p.Ala325=
ENST00000526760.5:c.*973C>A (BBS1)	ENSP00000432140.1:n.*973C>A
ENST00000526986.5:c.*21+202G>T (ZDHHC24)	ENSP00000431321.1:n.*21+202G>T
ENST00000527959.1:n.410C>A (BBS1)
ENST00000529766.5:n.1273C>A (BBS1)
ENST00000529955.5:n.1237C>A (BBS1)
ENST00000534073.5:c.*21+202G>T (ZDHHC24)	ENSP00000436503.1:n.*21+202G>T
ENST00000630659.2:c.*973C>A (BBS1)	ENSP00000486455.1:n.*973C>A
NM_024649.4:c.1266C>A (BBS1)	NP_078925.3:p.Ala422=
XM_005273874.3:c.*21+202G>T (ZDHHC24)	XP_005273931.1:n.*21+202G>T
XM_011544894.1:c.*21+202G>T (ZDHHC24)	XP_011543196.1:n.*21+202G>T
XM_011544895.1:c.560-2458G>T (ZDHHC24)	XP_011543197.1:n.560-2458G>T
XR_949860.1:n.686+202G>T (ZDHHC24)
NM_001348571.1:c.*21+202G>T (ZDHHC24)	NP_001335500.1:n.*21+202G>T
XM_005273874.4:c.*21+202G>T (ZDHHC24)	XP_005273931.1:n.*21+202G>T
XM_011544894.2:c.*21+202G>T (ZDHHC24)	XP_011543196.1:n.*21+202G>T
XR_001747823.2:n.741-2458G>T (ZDHHC24)
XR_949860.3:n.811+202G>T (ZDHHC24)
NM_024649.5:c.1266C>A (BBS1) MANE Select	NP_078925.3:p.Ala422=
NM_001348571.2:c.*21+202G>T (ZDHHC24)	NP_001335500.1:n.*21+202G>T