Canonical Allele Identifier: CA2658200612
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135233_26135234del , CM000664.2:g.26135233_26135234del GRCh38
NC_000002.11:g.26358102_26358103del , CM000664.1:g.26358102_26358103del GRCh37
NC_000002.10:g.26211606_26211607del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*212_*213del MANE Select ENSP00000264710.4:n.*212_*213del
ENST00000264710.4:c.*212_*213del ENSP00000264710.4:n.*212_*213del
ENST00000495146.5:n.1178_1179del
NM_016131.4:c.*212_*213del NP_057215.3:n.*212_*213del
XM_024452565.1:c.*212_*213del XP_024308333.1:n.*212_*213del
NM_016131.5:c.*212_*213del MANE Select NP_057215.3:n.*212_*213del