Canonical Allele Identifier: CA2658200753
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135446_26135452del , CM000664.2:g.26135446_26135452del GRCh38
NC_000002.11:g.26358315_26358321del , CM000664.1:g.26358315_26358321del GRCh37
NC_000002.10:g.26211819_26211825del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*425_*431del MANE Select ENSP00000264710.4:n.*425_*431del
ENST00000264710.4:c.*425_*431del ENSP00000264710.4:n.*425_*431del
NM_016131.4:c.*425_*431del NP_057215.3:n.*425_*431del
XM_024452565.1:c.*425_*431del XP_024308333.1:n.*425_*431del
NM_016131.5:c.*425_*431del MANE Select NP_057215.3:n.*425_*431del