Canonical Allele Identifier: CA1239676394
Gene: RAB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135357A= , CM000664.2:g.26135357A= GRCh38
NC_000002.11:g.26358226A= , CM000664.1:g.26358226A= GRCh37
NC_000002.10:g.26211730A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*336A= MANE Select ENSP00000264710.4:n.*336A=
ENST00000264710.4:c.*336A= ENSP00000264710.4:n.*336A=
NM_016131.4:c.*336A= NP_057215.3:n.*336A=
XM_024452565.1:c.*336A= XP_024308333.1:n.*336A=
NM_016131.5:c.*336A= MANE Select NP_057215.3:n.*336A=