Canonical Allele Identifier: CA1028595299
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1668088430
gnomAD v3: 2-26135299-TTC-T
gnomAD v4: 2-26135299-TTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135301_26135302del , CM000664.2:g.26135301_26135302del GRCh38
NC_000002.11:g.26358170_26358171del , CM000664.1:g.26358170_26358171del GRCh37
NC_000002.10:g.26211674_26211675del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*280_*281del MANE Select ENSP00000264710.4:n.*280_*281del
ENST00000264710.4:c.*280_*281del ENSP00000264710.4:n.*280_*281del
ENST00000495146.5:n.1246_1247del
NM_016131.4:c.*280_*281del NP_057215.3:n.*280_*281del
XM_024452565.1:c.*280_*281del XP_024308333.1:n.*280_*281del
NM_016131.5:c.*280_*281del MANE Select NP_057215.3:n.*280_*281del
Search 100 bp 5'
Search 100 bp 3'