Canonical Allele Identifier: CA349161353
Gene: BBS5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487814T>G , CM000664.2:g.169487814T>G GRCh38
NC_000002.11:g.170344324T>G , CM000664.1:g.170344324T>G GRCh37
NC_000002.10:g.170052570T>G NCBI36
NG_011567.1:g.13319T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.217T>G MANE Select ENSP00000295240.3:p.Tyr73Asp
ENST00000295240.7:c.217T>G ENSP00000295240.3:p.Tyr73Asp
ENST00000392663.6:c.217T>G ENSP00000376431.2:p.Tyr73Asp
ENST00000443151.1:c.143-173T>G ENSP00000406182.1:n.143-173T>G
ENST00000475571.1:n.53T>G
ENST00000513963.1:c.217T>G ENSP00000424363.1:p.Tyr73Asp
NM_152384.2:c.217T>G NP_689597.1:p.Tyr73Asp
NM_152384.3:c.217T>G MANE Select NP_689597.1:p.Tyr73Asp