Canonical Allele Identifier: CA2658200623
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135238-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135238T>G , CM000664.2:g.26135238T>G GRCh38
NC_000002.11:g.26358107T>G , CM000664.1:g.26358107T>G GRCh37
NC_000002.10:g.26211611T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*217T>G MANE Select ENSP00000264710.4:n.*217T>G
ENST00000264710.4:c.*217T>G ENSP00000264710.4:n.*217T>G
ENST00000495146.5:n.1183T>G
NM_016131.4:c.*217T>G NP_057215.3:n.*217T>G
XM_024452565.1:c.*217T>G XP_024308333.1:n.*217T>G
NM_016131.5:c.*217T>G MANE Select NP_057215.3:n.*217T>G
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