Canonical Allele Identifier: CA2749231026
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135200_26135205del , CM000664.2:g.26135200_26135205del GRCh38
NC_000002.11:g.26358069_26358074del , CM000664.1:g.26358069_26358074del GRCh37
NC_000002.10:g.26211573_26211578del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*179_*184del MANE Select ENSP00000264710.4:n.*179_*184del
ENST00000264710.4:c.*179_*184del ENSP00000264710.4:n.*179_*184del
ENST00000495146.5:n.1145_1150del
NM_016131.4:c.*179_*184del NP_057215.3:n.*179_*184del
XM_024452565.1:c.*179_*184del XP_024308333.1:n.*179_*184del
NM_016131.5:c.*179_*184del MANE Select NP_057215.3:n.*179_*184del