Canonical Allele Identifier: CA1239676238
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135168A= , CM000664.2:g.26135168A= GRCh38
NC_000002.11:g.26358037A= , CM000664.1:g.26358037A= GRCh37
NC_000002.10:g.26211541A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*147A= MANE Select ENSP00000264710.4:n.*147A=
ENST00000264710.4:c.*147A= ENSP00000264710.4:n.*147A=
ENST00000495146.5:n.1113A=
NM_016131.4:c.*147A= NP_057215.3:n.*147A=
XM_024452565.1:c.*147A= XP_024308333.1:n.*147A=
NM_016131.5:c.*147A= MANE Select NP_057215.3:n.*147A=