Canonical Allele Identifier: CA2658200534
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135160-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135160G>A , CM000664.2:g.26135160G>A GRCh38
NC_000002.11:g.26358029G>A , CM000664.1:g.26358029G>A GRCh37
NC_000002.10:g.26211533G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*139G>A MANE Select ENSP00000264710.4:n.*139G>A
ENST00000264710.4:c.*139G>A ENSP00000264710.4:n.*139G>A
ENST00000495146.5:n.1105G>A
NM_016131.4:c.*139G>A NP_057215.3:n.*139G>A
XM_024452565.1:c.*139G>A XP_024308333.1:n.*139G>A
NM_016131.5:c.*139G>A MANE Select NP_057215.3:n.*139G>A
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