Canonical Allele Identifier: CA1239676241
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135169T= , CM000664.2:g.26135169T= GRCh38
NC_000002.11:g.26358038T= , CM000664.1:g.26358038T= GRCh37
NC_000002.10:g.26211542T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*148T= MANE Select ENSP00000264710.4:n.*148T=
ENST00000264710.4:c.*148T= ENSP00000264710.4:n.*148T=
ENST00000495146.5:n.1114T=
NM_016131.4:c.*148T= NP_057215.3:n.*148T=
XM_024452565.1:c.*148T= XP_024308333.1:n.*148T=
NM_016131.5:c.*148T= MANE Select NP_057215.3:n.*148T=