Canonical Allele Identifier: CA2658200636
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135245-ATT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135249_26135250del , CM000664.2:g.26135249_26135250del GRCh38
NC_000002.11:g.26358118_26358119del , CM000664.1:g.26358118_26358119del GRCh37
NC_000002.10:g.26211622_26211623del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*228_*229del MANE Select ENSP00000264710.4:n.*228_*229del
ENST00000264710.4:c.*228_*229del ENSP00000264710.4:n.*228_*229del
ENST00000495146.5:n.1194_1195del
NM_016131.4:c.*228_*229del NP_057215.3:n.*228_*229del
XM_024452565.1:c.*228_*229del XP_024308333.1:n.*228_*229del
NM_016131.5:c.*228_*229del MANE Select NP_057215.3:n.*228_*229del
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