Canonical Allele Identifier: CA381455599

Gene: BBS1

Linked Data

• dbSNP Id: rs1590756387
• MyVariant Identifiers: chr11:g.66281890A>C (hg19) ; chr11:g.66514419A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514419A>C , CM000673.2:g.66514419A>C	GRCh38
NC_000011.9:g.66281890A>C , CM000673.1:g.66281890A>C	GRCh37
NC_000011.8:g.66038466A>C	NCBI36
NG_009093.1:g.8772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.173A>C MANE Select	ENSP00000317469.7:p.Asp58Ala
ENST00000318312.11:c.173A>C	ENSP00000317469.7:p.Asp58Ala
ENST00000393994.4:c.173A>C	ENSP00000377563.2:p.Asp58Ala
ENST00000419755.3:c.284A>C	ENSP00000398526.3:p.Asp95Ala
ENST00000455748.6:c.173A>C	ENSP00000405764.2:p.Asp58Ala
ENST00000524458.5:c.48A>C	ENSP00000436195.1:p.Gly16=
ENST00000524705.2:c.-20-87A>C	ENSP00000436927.1:n.-20-87A>C
ENST00000524907.5:n.163A>C
ENST00000525809.5:c.160-1121A>C	ENSP00000431187.1:n.160-1121A>C
ENST00000526035.5:c.138A>C	ENSP00000434197.1:p.Gly46=
ENST00000526760.5:c.138A>C	ENSP00000432140.1:p.Gly46=
ENST00000526815.5:c.83A>C	ENSP00000436860.1:p.Asp28Ala
ENST00000527251.5:c.48A>C	ENSP00000434360.1:p.Gly16=
ENST00000529766.5:n.180A>C
ENST00000529955.5:n.191A>C
ENST00000532908.5:c.138A>C	ENSP00000431866.1:p.Gly46=
ENST00000533557.5:c.138A>C	ENSP00000434619.1:p.Gly46=
ENST00000533644.5:c.173A>C	ENSP00000436073.1:p.Asp58Ala
ENST00000534730.5:n.185A>C
ENST00000630659.2:c.138A>C	ENSP00000486455.1:p.Gly46=
NM_024649.4:c.173A>C	NP_078925.3:p.Asp58Ala
NM_024649.5:c.173A>C MANE Select	NP_078925.3:p.Asp58Ala