Canonical Allele Identifier: CA2658200599
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135228del , CM000664.2:g.26135228del GRCh38
NC_000002.11:g.26358097del , CM000664.1:g.26358097del GRCh37
NC_000002.10:g.26211601del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*207del MANE Select ENSP00000264710.4:n.*207del
ENST00000264710.4:c.*207del ENSP00000264710.4:n.*207del
ENST00000495146.5:n.1173del
NM_016131.4:c.*207del NP_057215.3:n.*207del
XM_024452565.1:c.*207del XP_024308333.1:n.*207del
NM_016131.5:c.*207del MANE Select NP_057215.3:n.*207del