Canonical Allele Identifier: CA366761456
Gene: RAC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446365
ClinVar RCV Id: RCV003156718
MyVariant Identifiers: chr7:g.6431649C>A (hg19) chr7:g.6392018C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392018C>A , CM000669.2:g.6392018C>A GRCh38
NC_000007.13:g.6431649C>A , CM000669.1:g.6431649C>A GRCh37
NC_000007.12:g.6398174C>A NCBI36
NG_029431.1:g.22524C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.390C>A
ENST00000704002.1:c.301C>A ENSP00000515615.1:p.Arg101Ser
ENST00000704003.1:c.*155C>A ENSP00000515616.1:n.*155C>A
ENST00000348035.9:c.202C>A MANE Select ENSP00000258737.7:p.Arg68Ser
ENST00000348035.8:c.202C>A ENSP00000258737.7:p.Arg68Ser
ENST00000356142.4:c.202C>A ENSP00000348461.4:p.Arg68Ser
ENST00000488373.5:n.433C>A
ENST00000497741.5:n.218C>A
NM_006908.4:c.202C>A NP_008839.2:p.Arg68Ser
NM_018890.3:c.202C>A NP_061485.1:p.Arg68Ser
NM_006908.5:c.202C>A MANE Select NP_008839.2:p.Arg68Ser
NM_018890.4:c.202C>A NP_061485.1:p.Arg68Ser
Search 100 bp 5'
Search 100 bp 3'