Canonical Allele Identifier: CA381456001

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66281943G>C (hg19) ; chr11:g.66514472G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514472G>C , CM000673.2:g.66514472G>C	GRCh38
NC_000011.9:g.66281943G>C , CM000673.1:g.66281943G>C	GRCh37
NC_000011.8:g.66038519G>C	NCBI36
NG_009093.1:g.8825G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.226G>C MANE Select	ENSP00000317469.7:p.Val76Leu
ENST00000318312.11:c.226G>C	ENSP00000317469.7:p.Val76Leu
ENST00000393994.4:c.226G>C	ENSP00000377563.2:p.Val76Leu
ENST00000419755.3:c.337G>C	ENSP00000398526.3:p.Val113Leu
ENST00000455748.6:c.226G>C	ENSP00000405764.2:p.Val76Leu
ENST00000524458.5:c.101G>C	ENSP00000436195.1:p.Gly34Ala
ENST00000524705.2:c.-20-34G>C	ENSP00000436927.1:n.-20-34G>C
ENST00000524907.5:n.216G>C
ENST00000525809.5:c.160-1068G>C	ENSP00000431187.1:n.160-1068G>C
ENST00000526035.5:c.191G>C	ENSP00000434197.1:p.Gly64Ala
ENST00000526760.5:c.191G>C	ENSP00000432140.1:p.Gly64Ala
ENST00000526815.5:c.136G>C	ENSP00000436860.1:p.Val46Leu
ENST00000527251.5:c.101G>C	ENSP00000434360.1:p.Gly34Ala
ENST00000529766.5:n.233G>C
ENST00000529955.5:n.244G>C
ENST00000532908.5:c.191G>C	ENSP00000431866.1:p.Gly64Ala
ENST00000533430.5:n.4G>C
ENST00000533557.5:c.191G>C	ENSP00000434619.1:p.Gly64Ala
ENST00000533644.5:c.226G>C	ENSP00000436073.1:p.Val76Leu
ENST00000534730.5:n.238G>C
ENST00000630659.2:c.191G>C	ENSP00000486455.1:p.Gly64Ala
NM_024649.4:c.226G>C	NP_078925.3:p.Val76Leu
NM_024649.5:c.226G>C MANE Select	NP_078925.3:p.Val76Leu