Canonical Allele Identifier: CA1306468631
Gene: BBS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487822C= , CM000664.2:g.169487822C= GRCh38
NC_000002.11:g.170344332C= , CM000664.1:g.170344332C= GRCh37
NC_000002.10:g.170052578C= NCBI36
NG_011567.1:g.13327C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.225C= MANE Select ENSP00000295240.3:p.Cys75=
ENST00000295240.7:c.225C= ENSP00000295240.3:p.Cys75=
ENST00000392663.6:c.225C= ENSP00000376431.2:p.Cys75=
ENST00000443151.1:c.143-165C= ENSP00000406182.1:n.143-165C=
ENST00000475571.1:n.61C=
ENST00000513963.1:c.225C= ENSP00000424363.1:p.Cys75=
NM_152384.2:c.225C= NP_689597.1:p.Cys75=
NM_152384.3:c.225C= MANE Select NP_689597.1:p.Cys75=