Canonical Allele Identifier: CA1306468636

Gene: BBS5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169487832A= , CM000664.2:g.169487832A=	GRCh38
NC_000002.11:g.170344342A= , CM000664.1:g.170344342A=	GRCh37
NC_000002.10:g.170052588A=	NCBI36
NG_011567.1:g.13337A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295240.8:c.235A= MANE Select	ENSP00000295240.3:p.Ile79=
ENST00000295240.7:c.235A=	ENSP00000295240.3:p.Ile79=
ENST00000392663.6:c.235A=	ENSP00000376431.2:p.Ile79=
ENST00000443151.1:c.143-155A=	ENSP00000406182.1:n.143-155A=
ENST00000475571.1:n.71A=
ENST00000513963.1:c.235A=	ENSP00000424363.1:p.Ile79=
NM_152384.2:c.235A=	NP_689597.1:p.Ile79=
NM_152384.3:c.235A= MANE Select	NP_689597.1:p.Ile79=