Canonical Allele Identifier: CA2658200532
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135156-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135156A>C , CM000664.2:g.26135156A>C GRCh38
NC_000002.11:g.26358025A>C , CM000664.1:g.26358025A>C GRCh37
NC_000002.10:g.26211529A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*135A>C MANE Select ENSP00000264710.4:n.*135A>C
ENST00000264710.4:c.*135A>C ENSP00000264710.4:n.*135A>C
ENST00000495146.5:n.1101A>C
NM_016131.4:c.*135A>C NP_057215.3:n.*135A>C
XM_024452565.1:c.*135A>C XP_024308333.1:n.*135A>C
NM_016131.5:c.*135A>C MANE Select NP_057215.3:n.*135A>C
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