Canonical Allele Identifier: CA1306468630
Gene: BBS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487818A= , CM000664.2:g.169487818A= GRCh38
NC_000002.11:g.170344328A= , CM000664.1:g.170344328A= GRCh37
NC_000002.10:g.170052574A= NCBI36
NG_011567.1:g.13323A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295240.8:c.221A= MANE Select ENSP00000295240.3:p.Asn74=
ENST00000295240.7:c.221A= ENSP00000295240.3:p.Asn74=
ENST00000392663.6:c.221A= ENSP00000376431.2:p.Asn74=
ENST00000443151.1:c.143-169A= ENSP00000406182.1:n.143-169A=
ENST00000475571.1:n.57A=
ENST00000513963.1:c.221A= ENSP00000424363.1:p.Asn74=
NM_152384.2:c.221A= NP_689597.1:p.Asn74=
NM_152384.3:c.221A= MANE Select NP_689597.1:p.Asn74=