Canonical Allele Identifier: CA2658200639
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135246-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135246T>C , CM000664.2:g.26135246T>C GRCh38
NC_000002.11:g.26358115T>C , CM000664.1:g.26358115T>C GRCh37
NC_000002.10:g.26211619T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*225T>C MANE Select ENSP00000264710.4:n.*225T>C
ENST00000264710.4:c.*225T>C ENSP00000264710.4:n.*225T>C
ENST00000495146.5:n.1191T>C
NM_016131.4:c.*225T>C NP_057215.3:n.*225T>C
XM_024452565.1:c.*225T>C XP_024308333.1:n.*225T>C
NM_016131.5:c.*225T>C MANE Select NP_057215.3:n.*225T>C