Canonical Allele Identifier: CA1239676132
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135045C= , CM000664.2:g.26135045C= GRCh38
NC_000002.11:g.26357914C= , CM000664.1:g.26357914C= GRCh37
NC_000002.10:g.26211418C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*24C= MANE Select ENSP00000264710.4:n.*24C=
ENST00000264710.4:c.*24C= ENSP00000264710.4:n.*24C=
ENST00000473035.1:n.548C=
ENST00000495146.5:n.990C=
NM_016131.4:c.*24C= NP_057215.3:n.*24C=
XM_024452565.1:c.*24C= XP_024308333.1:n.*24C=
NM_016131.5:c.*24C= MANE Select NP_057215.3:n.*24C=