Canonical Allele Identifier: CA2658200583
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135213_26135216dup , CM000664.2:g.26135213_26135216dup GRCh38
NC_000002.11:g.26358082_26358085dup , CM000664.1:g.26358082_26358085dup GRCh37
NC_000002.10:g.26211586_26211589dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*192_*195dup MANE Select ENSP00000264710.4:n.*192_*195dup
ENST00000264710.4:c.*192_*195dup ENSP00000264710.4:n.*192_*195dup
ENST00000495146.5:n.1158_1161dup
NM_016131.4:c.*192_*195dup NP_057215.3:n.*192_*195dup
XM_024452565.1:c.*192_*195dup XP_024308333.1:n.*192_*195dup
NM_016131.5:c.*192_*195dup MANE Select NP_057215.3:n.*192_*195dup