Canonical Allele Identifier: CA1239676171

Gene: RAB10

Linked Data

• dbSNP Id: rs1668081845

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26135080A>C , CM000664.2:g.26135080A>C	GRCh38
NC_000002.11:g.26357949A>C , CM000664.1:g.26357949A>C	GRCh37
NC_000002.10:g.26211453A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264710.5:c.*59A>C MANE Select	ENSP00000264710.4:n.*59A>C
ENST00000264710.4:c.*59A>C	ENSP00000264710.4:n.*59A>C
ENST00000495146.5:n.1025A>C
NM_016131.4:c.*59A>C	NP_057215.3:n.*59A>C
XM_024452565.1:c.*59A>C	XP_024308333.1:n.*59A>C
NM_016131.5:c.*59A>C MANE Select	NP_057215.3:n.*59A>C