Canonical Allele Identifier: CA2658200649
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135250-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135253del , CM000664.2:g.26135253del GRCh38
NC_000002.11:g.26358122del , CM000664.1:g.26358122del GRCh37
NC_000002.10:g.26211626del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*232del MANE Select ENSP00000264710.4:n.*232del
ENST00000264710.4:c.*232del ENSP00000264710.4:n.*232del
ENST00000495146.5:n.1198del
NM_016131.4:c.*232del NP_057215.3:n.*232del
XM_024452565.1:c.*232del XP_024308333.1:n.*232del
NM_016131.5:c.*232del MANE Select NP_057215.3:n.*232del
Search 100 bp 5'
Search 100 bp 3'