Canonical Allele Identifier: CA1685476389
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391984G= , CM000669.2:g.6391984G= GRCh38
NC_000007.13:g.6431615G= , CM000669.1:g.6431615G= GRCh37
NC_000007.12:g.6398140G= NCBI36
NG_029431.1:g.22490G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.356G=
ENST00000704002.1:c.267G= ENSP00000515615.1:p.Trp89=
ENST00000704003.1:c.*121G= ENSP00000515616.1:n.*121G=
ENST00000348035.9:c.168G= MANE Select ENSP00000258737.7:p.Trp56=
ENST00000348035.8:c.168G= ENSP00000258737.7:p.Trp56=
ENST00000356142.4:c.168G= ENSP00000348461.4:p.Trp56=
ENST00000488373.5:n.399G=
ENST00000497741.5:n.184G=
NM_006908.4:c.168G= NP_008839.2:p.Trp56=
NM_018890.3:c.168G= NP_061485.1:p.Trp56=
NM_006908.5:c.168G= MANE Select NP_008839.2:p.Trp56=
NM_018890.4:c.168G= NP_061485.1:p.Trp56=