Canonical Allele Identifier: CA2047353484
Gene: BBS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346793_76346795delinsCTA , CM000674.2:g.76346793_76346795delinsCTA GRCh38
NC_000012.11:g.76740573_76740575delinsCTA , CM000674.1:g.76740573_76740575delinsCTA GRCh37
NC_000012.10:g.75264704_75264706delinsCTA NCBI36
NG_016357.1:g.6648_6650delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.1190_1192delinsTAG MANE Select ENSP00000497413.1:p.Ile397=
ENST00000393262.3:c.1190_1192delinsTAG ENSP00000376946.3:p.Ile397=
NM_024685.3:c.1190_1192delinsTAG NP_078961.3:p.Ile397=
NM_024685.4:c.1190_1192delinsTAG MANE Select NP_078961.3:p.Ile397=