Canonical Allele Identifier: CA2658200707
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135316-A-T

Genomic Alleles

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

Transcript Alleles

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