Canonical Allele Identifier: CA6123821

Gene: BBS1 ZDHHC24

Linked Data

• ClinVar Variation Id: 393063
• ClinVar RCV Id: RCV003932696
• dbSNP Id: rs770105141
• ExAC: 11:66298485 C / T
• gnomAD v2: 11-66298485-C-T
• gnomAD v3: 11-66531014-C-T
• gnomAD v4: 11-66531014-C-T
• MyVariant Identifiers: chr11:g.66298485C>T (hg19) ; chr11:g.66531014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66531014C>T , CM000673.2:g.66531014C>T	GRCh38
NC_000011.9:g.66298485C>T , CM000673.1:g.66298485C>T	GRCh37
NC_000011.8:g.66055061C>T	NCBI36
NG_009093.1:g.25367C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.1594C>T (BBS1) MANE Select	ENSP00000317469.7:p.Arg532Trp
ENST00000318312.11:c.1594C>T (BBS1)	ENSP00000317469.7:p.Arg532Trp
ENST00000393994.4:c.1207C>T (BBS1)	ENSP00000377563.2:p.Arg403Trp
ENST00000419755.3:c.1705C>T	ENSP00000398526.3:p.Arg569Trp
ENST00000455748.6:c.1303C>T (BBS1)	ENSP00000405764.2:p.Arg435Trp
ENST00000526760.5:c.*1301C>T (BBS1)	ENSP00000432140.1:n.*1301C>T
ENST00000526986.5:c.560-1526G>A (ZDHHC24)	ENSP00000431321.1:n.560-1526G>A
ENST00000529955.5:n.1565C>T (BBS1)
ENST00000534073.5:c.560-4008G>A (ZDHHC24)	ENSP00000436503.1:n.560-4008G>A
ENST00000630659.2:c.*1301C>T (BBS1)	ENSP00000486455.1:n.*1301C>T
NM_024649.4:c.1594C>T (BBS1)	NP_078925.3:p.Arg532Trp
XM_005273874.3:c.560-4008G>A (ZDHHC24)	XP_005273931.1:n.560-4008G>A
XM_011544891.1:c.560-1526G>A (ZDHHC24)	XP_011543193.1:n.560-1526G>A
XM_011544894.1:c.560-4008G>A (ZDHHC24)	XP_011543196.1:n.560-4008G>A
XM_011544895.1:c.560-6738G>A (ZDHHC24)	XP_011543197.1:n.560-6738G>A
XR_949860.1:n.616-4008G>A (ZDHHC24)
NM_001348571.1:c.560-1526G>A (ZDHHC24)	NP_001335500.1:n.560-1526G>A
XM_005273874.4:c.560-4008G>A (ZDHHC24)	XP_005273931.1:n.560-4008G>A
XM_011544894.2:c.560-4008G>A (ZDHHC24)	XP_011543196.1:n.560-4008G>A
XR_001747823.2:n.741-6738G>A (ZDHHC24)
XR_949860.3:n.741-4008G>A (ZDHHC24)
NM_024649.5:c.1594C>T (BBS1) MANE Select	NP_078925.3:p.Arg532Trp
NM_001348571.2:c.560-1526G>A (ZDHHC24)	NP_001335500.1:n.560-1526G>A