Canonical Allele Identifier: CA2576696164
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135095del , CM000664.2:g.26135095del GRCh38
NC_000002.11:g.26357964del , CM000664.1:g.26357964del GRCh37
NC_000002.10:g.26211468del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*74del MANE Select ENSP00000264710.4:n.*74del
ENST00000264710.4:c.*74del ENSP00000264710.4:n.*74del
ENST00000495146.5:n.1040del
NM_016131.4:c.*74del NP_057215.3:n.*74del
XM_024452565.1:c.*74del XP_024308333.1:n.*74del
NM_016131.5:c.*74del MANE Select NP_057215.3:n.*74del