Canonical Allele Identifier: CA2658200598
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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