Canonical Allele Identifier: CA2658200652
Gene: RAB10 HGNC NCBI

Linked Data

gnomAD v4: 2-26135252-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135252A>T , CM000664.2:g.26135252A>T GRCh38
NC_000002.11:g.26358121A>T , CM000664.1:g.26358121A>T GRCh37
NC_000002.10:g.26211625A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*231A>T MANE Select ENSP00000264710.4:n.*231A>T
ENST00000264710.4:c.*231A>T ENSP00000264710.4:n.*231A>T
ENST00000495146.5:n.1197A>T
NM_016131.4:c.*231A>T NP_057215.3:n.*231A>T
XM_024452565.1:c.*231A>T XP_024308333.1:n.*231A>T
NM_016131.5:c.*231A>T MANE Select NP_057215.3:n.*231A>T