Canonical Allele Identifier: CA2658200577
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135205_26135216del , CM000664.2:g.26135205_26135216del GRCh38
NC_000002.11:g.26358074_26358085del , CM000664.1:g.26358074_26358085del GRCh37
NC_000002.10:g.26211578_26211589del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*184_*195del MANE Select ENSP00000264710.4:n.*184_*195del
ENST00000264710.4:c.*184_*195del ENSP00000264710.4:n.*184_*195del
ENST00000495146.5:n.1150_1161del
NM_016131.4:c.*184_*195del NP_057215.3:n.*184_*195del
XM_024452565.1:c.*184_*195del XP_024308333.1:n.*184_*195del
NM_016131.5:c.*184_*195del MANE Select NP_057215.3:n.*184_*195del