Canonical Allele Identifier: CA2658200695
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135296-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135296C>T , CM000664.2:g.26135296C>T GRCh38
NC_000002.11:g.26358165C>T , CM000664.1:g.26358165C>T GRCh37
NC_000002.10:g.26211669C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*275C>T MANE Select ENSP00000264710.4:n.*275C>T
ENST00000264710.4:c.*275C>T ENSP00000264710.4:n.*275C>T
ENST00000495146.5:n.1241C>T
NM_016131.4:c.*275C>T NP_057215.3:n.*275C>T
XM_024452565.1:c.*275C>T XP_024308333.1:n.*275C>T
NM_016131.5:c.*275C>T MANE Select NP_057215.3:n.*275C>T