Canonical Allele Identifier: CA531389195
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1229428371
gnomAD v2: 2-26358056-CTT-C
gnomAD v3: 2-26135187-CTT-C
gnomAD v4: 2-26135187-CTT-C
MyVariant Identifiers: chr2:g.26358057_26358058del (hg19) chr2:g.26135188_26135189del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135189_26135190del , CM000664.2:g.26135189_26135190del GRCh38
NC_000002.11:g.26358058_26358059del , CM000664.1:g.26358058_26358059del GRCh37
NC_000002.10:g.26211562_26211563del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*168_*169del MANE Select ENSP00000264710.4:n.*168_*169del
ENST00000264710.4:c.*168_*169del ENSP00000264710.4:n.*168_*169del
ENST00000495146.5:n.1134_1135del
NM_016131.4:c.*168_*169del NP_057215.3:n.*168_*169del
XM_024452565.1:c.*168_*169del XP_024308333.1:n.*168_*169del
NM_016131.5:c.*168_*169del MANE Select NP_057215.3:n.*168_*169del
Search 100 bp 5'
Search 100 bp 3'