Canonical Allele Identifier: CA1239676244
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135172G= , CM000664.2:g.26135172G= GRCh38
NC_000002.11:g.26358041G= , CM000664.1:g.26358041G= GRCh37
NC_000002.10:g.26211545G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*151G= MANE Select ENSP00000264710.4:n.*151G=
ENST00000264710.4:c.*151G= ENSP00000264710.4:n.*151G=
ENST00000495146.5:n.1117G=
NM_016131.4:c.*151G= NP_057215.3:n.*151G=
XM_024452565.1:c.*151G= XP_024308333.1:n.*151G=
NM_016131.5:c.*151G= MANE Select NP_057215.3:n.*151G=