Canonical Allele Identifier: CA453648277
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431651C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392020C>G , CM000669.2:g.6392020C>G GRCh38
NC_000007.13:g.6431651C>G , CM000669.1:g.6431651C>G GRCh37
NC_000007.12:g.6398176C>G NCBI36
NG_029431.1:g.22526C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.392C>G
ENST00000704002.1:c.303C>G ENSP00000515615.1:p.Arg101=
ENST00000704003.1:c.*157C>G ENSP00000515616.1:n.*157C>G
ENST00000348035.9:c.204C>G MANE Select ENSP00000258737.7:p.Arg68=
ENST00000348035.8:c.204C>G ENSP00000258737.7:p.Arg68=
ENST00000356142.4:c.204C>G ENSP00000348461.4:p.Arg68=
ENST00000488373.5:n.435C>G
ENST00000497741.5:n.220C>G
NM_006908.4:c.204C>G NP_008839.2:p.Arg68=
NM_018890.3:c.204C>G NP_061485.1:p.Arg68=
NM_006908.5:c.204C>G MANE Select NP_008839.2:p.Arg68=
NM_018890.4:c.204C>G NP_061485.1:p.Arg68=