Canonical Allele Identifier: CA2533848435
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135193_26135195del , CM000664.2:g.26135193_26135195del GRCh38
NC_000002.11:g.26358062_26358064del , CM000664.1:g.26358062_26358064del GRCh37
NC_000002.10:g.26211566_26211568del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*172_*174del MANE Select ENSP00000264710.4:n.*172_*174del
ENST00000264710.4:c.*172_*174del ENSP00000264710.4:n.*172_*174del
ENST00000495146.5:n.1138_1140del
NM_016131.4:c.*172_*174del NP_057215.3:n.*172_*174del
XM_024452565.1:c.*172_*174del XP_024308333.1:n.*172_*174del
NM_016131.5:c.*172_*174del MANE Select NP_057215.3:n.*172_*174del