Canonical Allele Identifier: CA1239676140
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135053T= , CM000664.2:g.26135053T= GRCh38
NC_000002.11:g.26357922T= , CM000664.1:g.26357922T= GRCh37
NC_000002.10:g.26211426T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*32T= MANE Select ENSP00000264710.4:n.*32T=
ENST00000264710.4:c.*32T= ENSP00000264710.4:n.*32T=
ENST00000473035.1:n.556T=
ENST00000495146.5:n.998T=
NM_016131.4:c.*32T= NP_057215.3:n.*32T=
XM_024452565.1:c.*32T= XP_024308333.1:n.*32T=
NM_016131.5:c.*32T= MANE Select NP_057215.3:n.*32T=