Canonical Allele Identifier: CA2573148987
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1366812
ClinVar RCV Id: RCV001944862
dbSNP Id: rs2136089877

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346170_76346171del , CM000674.2:g.76346170_76346171del GRCh38
NC_000012.11:g.76739950_76739951del , CM000674.1:g.76739950_76739951del GRCh37
NC_000012.10:g.75264081_75264082del NCBI36
NG_016357.1:g.7272_7273del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1814_1815del MANE Select ENSP00000497413.1:p.Asn605IlefsTer2
ENST00000393262.3:c.1814_1815del ENSP00000376946.3:p.Asn605IlefsTer2
NM_024685.3:c.1814_1815del NP_078961.3:p.Asn605IlefsTer2
NM_024685.4:c.1814_1815del MANE Select NP_078961.3:p.Asn605IlefsTer2