Canonical Allele Identifier: CA2658200517
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135140-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135140C>T , CM000664.2:g.26135140C>T GRCh38
NC_000002.11:g.26358009C>T , CM000664.1:g.26358009C>T GRCh37
NC_000002.10:g.26211513C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*119C>T MANE Select ENSP00000264710.4:n.*119C>T
ENST00000264710.4:c.*119C>T ENSP00000264710.4:n.*119C>T
ENST00000495146.5:n.1085C>T
NM_016131.4:c.*119C>T NP_057215.3:n.*119C>T
XM_024452565.1:c.*119C>T XP_024308333.1:n.*119C>T
NM_016131.5:c.*119C>T MANE Select NP_057215.3:n.*119C>T
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