Canonical Allele Identifier: CA2844987394
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135299T>C , CM000664.2:g.26135299T>C GRCh38
NC_000002.11:g.26358168T>C , CM000664.1:g.26358168T>C GRCh37
NC_000002.10:g.26211672T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*278T>C MANE Select ENSP00000264710.4:n.*278T>C
ENST00000264710.4:c.*278T>C ENSP00000264710.4:n.*278T>C
ENST00000495146.5:n.1244T>C
NM_016131.4:c.*278T>C NP_057215.3:n.*278T>C
XM_024452565.1:c.*278T>C XP_024308333.1:n.*278T>C
NM_016131.5:c.*278T>C MANE Select NP_057215.3:n.*278T>C