Canonical Allele Identifier: CA381455851

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66281920T>C (hg19) ; chr11:g.66514449T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514449T>C , CM000673.2:g.66514449T>C	GRCh38
NC_000011.9:g.66281920T>C , CM000673.1:g.66281920T>C	GRCh37
NC_000011.8:g.66038496T>C	NCBI36
NG_009093.1:g.8802T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.203T>C MANE Select	ENSP00000317469.7:p.Leu68Pro
ENST00000318312.11:c.203T>C	ENSP00000317469.7:p.Leu68Pro
ENST00000393994.4:c.203T>C	ENSP00000377563.2:p.Leu68Pro
ENST00000419755.3:c.314T>C	ENSP00000398526.3:p.Leu105Pro
ENST00000455748.6:c.203T>C	ENSP00000405764.2:p.Leu68Pro
ENST00000524458.5:c.78T>C	ENSP00000436195.1:p.Pro26=
ENST00000524705.2:c.-20-57T>C	ENSP00000436927.1:n.-20-57T>C
ENST00000524907.5:n.193T>C
ENST00000525809.5:c.160-1091T>C	ENSP00000431187.1:n.160-1091T>C
ENST00000526035.5:c.168T>C	ENSP00000434197.1:p.Pro56=
ENST00000526760.5:c.168T>C	ENSP00000432140.1:p.Pro56=
ENST00000526815.5:c.113T>C	ENSP00000436860.1:p.Leu38Pro
ENST00000527251.5:c.78T>C	ENSP00000434360.1:p.Pro26=
ENST00000529766.5:n.210T>C
ENST00000529955.5:n.221T>C
ENST00000532908.5:c.168T>C	ENSP00000431866.1:p.Pro56=
ENST00000533557.5:c.168T>C	ENSP00000434619.1:p.Pro56=
ENST00000533644.5:c.203T>C	ENSP00000436073.1:p.Leu68Pro
ENST00000534730.5:n.215T>C
ENST00000630659.2:c.168T>C	ENSP00000486455.1:p.Pro56=
NM_024649.4:c.203T>C	NP_078925.3:p.Leu68Pro
NM_024649.5:c.203T>C MANE Select	NP_078925.3:p.Leu68Pro