Canonical Allele Identifier: CA1306468628
Gene: BBS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487810_169487811delinsCG , CM000664.2:g.169487810_169487811delinsCG GRCh38
NC_000002.11:g.170344320_170344321delinsCG , CM000664.1:g.170344320_170344321delinsCG GRCh37
NC_000002.10:g.170052566_170052567delinsCG NCBI36
NG_011567.1:g.13315_13316delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.213_214delinsCG MANE Select ENSP00000295240.3:p.Val71=
ENST00000295240.7:c.213_214delinsCG ENSP00000295240.3:p.Val71=
ENST00000392663.6:c.213_214delinsCG ENSP00000376431.2:p.Val71=
ENST00000443151.1:c.143-177_143-176delinsCG ENSP00000406182.1:n.143-177_143-176delins...
ENST00000475571.1:n.49_50delinsCG
ENST00000513963.1:c.213_214delinsCG ENSP00000424363.1:p.Val71=
NM_152384.2:c.213_214delinsCG NP_689597.1:p.Val71=
NM_152384.3:c.213_214delinsCG MANE Select NP_689597.1:p.Val71=