Canonical Allele Identifier: CA1239676337
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135303_26135309delinsTATCAAC , CM000664.2:g.26135303_26135309delinsTATCAAC GRCh38
NC_000002.11:g.26358172_26358178delinsTATCAAC , CM000664.1:g.26358172_26358178delinsTATCAAC GRCh37
NC_000002.10:g.26211676_26211682delinsTATCAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*282_*288delinsTATCAAC MANE Select ENSP00000264710.4:n.*282_*288delinsTATCAA...
ENST00000264710.4:c.*282_*288delinsTATCAAC ENSP00000264710.4:n.*282_*288delinsTATCAA...
ENST00000495146.5:n.1248_1254delinsTATCAAC
NM_016131.4:c.*282_*288delinsTATCAAC NP_057215.3:n.*282_*288delinsTATCAAC
XM_024452565.1:c.*282_*288delinsTATCAAC XP_024308333.1:n.*282_*288delinsTATCAAC
NM_016131.5:c.*282_*288delinsTATCAAC MANE Select NP_057215.3:n.*282_*288delinsTATCAAC