Canonical Allele Identifier: CA349161357
Gene: BBS5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169487815A>C , CM000664.2:g.169487815A>C GRCh38
NC_000002.11:g.170344325A>C , CM000664.1:g.170344325A>C GRCh37
NC_000002.10:g.170052571A>C NCBI36
NG_011567.1:g.13320A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295240.8:c.218A>C MANE Select ENSP00000295240.3:p.Tyr73Ser
ENST00000295240.7:c.218A>C ENSP00000295240.3:p.Tyr73Ser
ENST00000392663.6:c.218A>C ENSP00000376431.2:p.Tyr73Ser
ENST00000443151.1:c.143-172A>C ENSP00000406182.1:n.143-172A>C
ENST00000475571.1:n.54A>C
ENST00000513963.1:c.218A>C ENSP00000424363.1:p.Tyr73Ser
NM_152384.2:c.218A>C NP_689597.1:p.Tyr73Ser
NM_152384.3:c.218A>C MANE Select NP_689597.1:p.Tyr73Ser