Canonical Allele Identifier: CA2658200697
Gene: RAB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135297del , CM000664.2:g.26135297del GRCh38
NC_000002.11:g.26358166del , CM000664.1:g.26358166del GRCh37
NC_000002.10:g.26211670del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*276del MANE Select ENSP00000264710.4:n.*276del
ENST00000264710.4:c.*276del ENSP00000264710.4:n.*276del
ENST00000495146.5:n.1242del
NM_016131.4:c.*276del NP_057215.3:n.*276del
XM_024452565.1:c.*276del XP_024308333.1:n.*276del
NM_016131.5:c.*276del MANE Select NP_057215.3:n.*276del