Canonical Allele Identifier: CA1239676402
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135391C= , CM000664.2:g.26135391C= GRCh38
NC_000002.11:g.26358260C= , CM000664.1:g.26358260C= GRCh37
NC_000002.10:g.26211764C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*370C= MANE Select ENSP00000264710.4:n.*370C=
ENST00000264710.4:c.*370C= ENSP00000264710.4:n.*370C=
NM_016131.4:c.*370C= NP_057215.3:n.*370C=
XM_024452565.1:c.*370C= XP_024308333.1:n.*370C=
NM_016131.5:c.*370C= MANE Select NP_057215.3:n.*370C=