Canonical Allele Identifier: CA366766822
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6402337G>A , CM000669.2:g.6402337G>A GRCh38
NC_000007.13:g.6441968G>A , CM000669.1:g.6441968G>A GRCh37
NC_000007.12:g.6408493G>A NCBI36
NG_029431.1:g.32843G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704002.1:c.569G>A ENSP00000515615.1:p.Cys190Tyr
ENST00000704003.1:c.*423G>A ENSP00000515616.1:n.*423G>A
ENST00000348035.9:c.470G>A MANE Select ENSP00000258737.7:p.Cys157Tyr
ENST00000348035.8:c.470G>A ENSP00000258737.7:p.Cys157Tyr
ENST00000356142.4:c.527G>A ENSP00000348461.4:p.Cys176Tyr
ENST00000473564.1:n.548G>A
ENST00000488373.5:n.701G>A
ENST00000495499.1:n.432G>A
ENST00000497741.5:n.486G>A
NM_006908.4:c.470G>A NP_008839.2:p.Cys157Tyr
NM_018890.3:c.527G>A NP_061485.1:p.Cys176Tyr
NM_006908.5:c.470G>A MANE Select NP_008839.2:p.Cys157Tyr
NM_018890.4:c.527G>A NP_061485.1:p.Cys176Tyr