Canonical Allele Identifier: CA381457368

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66283049G>C (hg19) ; chr11:g.66515578G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515578G>C , CM000673.2:g.66515578G>C	GRCh38
NC_000011.9:g.66283049G>C , CM000673.1:g.66283049G>C	GRCh37
NC_000011.8:g.66039625G>C	NCBI36
NG_009093.1:g.9931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.471G>C MANE Select	ENSP00000317469.7:p.Glu157Asp
ENST00000318312.11:c.471G>C	ENSP00000317469.7:p.Glu157Asp
ENST00000393994.4:c.471G>C	ENSP00000377563.2:p.Glu157Asp
ENST00000419755.3:c.582G>C	ENSP00000398526.3:p.Glu194Asp
ENST00000455748.6:c.432+900G>C	ENSP00000405764.2:n.432+900G>C
ENST00000524458.5:c.*140-115G>C	ENSP00000436195.1:n.*140-115G>C
ENST00000524705.2:c.192G>C	ENSP00000436927.1:p.Glu64Asp
ENST00000524907.5:n.461G>C
ENST00000525809.5:c.198G>C	ENSP00000431187.1:p.Glu66Asp
ENST00000526035.5:c.*178G>C	ENSP00000434197.1:n.*178G>C
ENST00000526760.5:c.*178G>C	ENSP00000432140.1:n.*178G>C
ENST00000527251.5:c.*178G>C	ENSP00000434360.1:n.*178G>C
ENST00000529766.5:n.478G>C
ENST00000529953.5:n.123G>C
ENST00000529955.5:n.451-115G>C
ENST00000532908.5:c.*140-115G>C	ENSP00000431866.1:n.*140-115G>C
ENST00000533430.5:n.249G>C
ENST00000533557.5:c.*140-115G>C	ENSP00000434619.1:n.*140-115G>C
ENST00000533644.5:c.433-115G>C	ENSP00000436073.1:n.433-115G>C
ENST00000534730.5:n.483G>C
ENST00000630659.2:c.*178G>C	ENSP00000486455.1:n.*178G>C
NM_024649.4:c.471G>C	NP_078925.3:p.Glu157Asp
NM_024649.5:c.471G>C MANE Select	NP_078925.3:p.Glu157Asp