Canonical Allele Identifier: CA1239676269
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135209_26135210delinsCA , CM000664.2:g.26135209_26135210delinsCA GRCh38
NC_000002.11:g.26358078_26358079delinsCA , CM000664.1:g.26358078_26358079delinsCA GRCh37
NC_000002.10:g.26211582_26211583delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*188_*189delinsCA MANE Select ENSP00000264710.4:n.*188_*189delinsCA
ENST00000264710.4:c.*188_*189delinsCA ENSP00000264710.4:n.*188_*189delinsCA
ENST00000495146.5:n.1154_1155delinsCA
NM_016131.4:c.*188_*189delinsCA NP_057215.3:n.*188_*189delinsCA
XM_024452565.1:c.*188_*189delinsCA XP_024308333.1:n.*188_*189delinsCA
NM_016131.5:c.*188_*189delinsCA MANE Select NP_057215.3:n.*188_*189delinsCA