Canonical Allele Identifier: CA1239676335
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135299_26135301delinsTTC , CM000664.2:g.26135299_26135301delinsTTC GRCh38
NC_000002.11:g.26358168_26358170delinsTTC , CM000664.1:g.26358168_26358170delinsTTC GRCh37
NC_000002.10:g.26211672_26211674delinsTTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*278_*280delinsTTC MANE Select ENSP00000264710.4:n.*278_*280delinsTTC
ENST00000264710.4:c.*278_*280delinsTTC ENSP00000264710.4:n.*278_*280delinsTTC
ENST00000495146.5:n.1244_1246delinsTTC
NM_016131.4:c.*278_*280delinsTTC NP_057215.3:n.*278_*280delinsTTC
XM_024452565.1:c.*278_*280delinsTTC XP_024308333.1:n.*278_*280delinsTTC
NM_016131.5:c.*278_*280delinsTTC MANE Select NP_057215.3:n.*278_*280delinsTTC