Canonical Allele Identifier: CA2658200708
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135316-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135316A>G , CM000664.2:g.26135316A>G GRCh38
NC_000002.11:g.26358185A>G , CM000664.1:g.26358185A>G GRCh37
NC_000002.10:g.26211689A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*295A>G MANE Select ENSP00000264710.4:n.*295A>G
ENST00000264710.4:c.*295A>G ENSP00000264710.4:n.*295A>G
ENST00000495146.5:n.1261A>G
NM_016131.4:c.*295A>G NP_057215.3:n.*295A>G
XM_024452565.1:c.*295A>G XP_024308333.1:n.*295A>G
NM_016131.5:c.*295A>G MANE Select NP_057215.3:n.*295A>G