Canonical Allele Identifier: CA381455597

Gene: BBS1

Linked Data

• gnomAD v4: 11-66514418-G-T
• MyVariant Identifiers: chr11:g.66281889G>T (hg19) ; chr11:g.66514418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514418G>T , CM000673.2:g.66514418G>T	GRCh38
NC_000011.9:g.66281889G>T , CM000673.1:g.66281889G>T	GRCh37
NC_000011.8:g.66038465G>T	NCBI36
NG_009093.1:g.8771G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.172G>T MANE Select	ENSP00000317469.7:p.Asp58Tyr
ENST00000318312.11:c.172G>T	ENSP00000317469.7:p.Asp58Tyr
ENST00000393994.4:c.172G>T	ENSP00000377563.2:p.Asp58Tyr
ENST00000419755.3:c.283G>T	ENSP00000398526.3:p.Asp95Tyr
ENST00000455748.6:c.172G>T	ENSP00000405764.2:p.Asp58Tyr
ENST00000524458.5:c.47G>T	ENSP00000436195.1:p.Gly16Val
ENST00000524705.2:c.-20-88G>T	ENSP00000436927.1:n.-20-88G>T
ENST00000524907.5:n.162G>T
ENST00000525809.5:c.160-1122G>T	ENSP00000431187.1:n.160-1122G>T
ENST00000526035.5:c.137G>T	ENSP00000434197.1:p.Gly46Val
ENST00000526760.5:c.137G>T	ENSP00000432140.1:p.Gly46Val
ENST00000526815.5:c.82G>T	ENSP00000436860.1:p.Asp28Tyr
ENST00000527251.5:c.47G>T	ENSP00000434360.1:p.Gly16Val
ENST00000529766.5:n.179G>T
ENST00000529955.5:n.190G>T
ENST00000532908.5:c.137G>T	ENSP00000431866.1:p.Gly46Val
ENST00000533557.5:c.137G>T	ENSP00000434619.1:p.Gly46Val
ENST00000533644.5:c.172G>T	ENSP00000436073.1:p.Asp58Tyr
ENST00000534730.5:n.184G>T
ENST00000630659.2:c.137G>T	ENSP00000486455.1:p.Gly46Val
NM_024649.4:c.172G>T	NP_078925.3:p.Asp58Tyr
NM_024649.5:c.172G>T MANE Select	NP_078925.3:p.Asp58Tyr