Canonical Allele Identifier: CA2658200712
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135323-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135323G>A , CM000664.2:g.26135323G>A GRCh38
NC_000002.11:g.26358192G>A , CM000664.1:g.26358192G>A GRCh37
NC_000002.10:g.26211696G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*302G>A MANE Select ENSP00000264710.4:n.*302G>A
ENST00000264710.4:c.*302G>A ENSP00000264710.4:n.*302G>A
ENST00000495146.5:n.1268G>A
NM_016131.4:c.*302G>A NP_057215.3:n.*302G>A
XM_024452565.1:c.*302G>A XP_024308333.1:n.*302G>A
NM_016131.5:c.*302G>A MANE Select NP_057215.3:n.*302G>A