Canonical Allele Identifier: CA767263142
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs140479291
gnomAD v4: 2-26135209-C-CA
MyVariant Identifiers: chr2:g.26358078_26358079insA (hg19) chr2:g.26135209_26135210insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135216dup , CM000664.2:g.26135216dup GRCh38
NC_000002.11:g.26358085dup , CM000664.1:g.26358085dup GRCh37
NC_000002.10:g.26211589dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*195dup MANE Select ENSP00000264710.4:n.*195dup
ENST00000264710.4:c.*195dup ENSP00000264710.4:n.*195dup
ENST00000495146.5:n.1161dup
NM_016131.4:c.*195dup NP_057215.3:n.*195dup
XM_024452565.1:c.*195dup XP_024308333.1:n.*195dup
NM_016131.5:c.*195dup MANE Select NP_057215.3:n.*195dup
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