Canonical Allele Identifier: CA767263172
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1158749337
gnomAD v3: 2-26135258-CTTGCTCAGCTCAACTGCA-C
gnomAD v4: 2-26135258-CTTGCTCAGCTCAACTGCA-C
MyVariant Identifiers: chr2:g.26358128_26358145del (hg19) chr2:g.26135259_26135276del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135261_26135278del , CM000664.2:g.26135261_26135278del GRCh38
NC_000002.11:g.26358130_26358147del , CM000664.1:g.26358130_26358147del GRCh37
NC_000002.10:g.26211634_26211651del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*240_*257del MANE Select ENSP00000264710.4:n.*240_*257del
ENST00000264710.4:c.*240_*257del ENSP00000264710.4:n.*240_*257del
ENST00000495146.5:n.1206_1223del
NM_016131.4:c.*240_*257del NP_057215.3:n.*240_*257del
XM_024452565.1:c.*240_*257del XP_024308333.1:n.*240_*257del
NM_016131.5:c.*240_*257del MANE Select NP_057215.3:n.*240_*257del
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