Canonical Allele Identifier: CA1685476422
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392023C= , CM000669.2:g.6392023C= GRCh38
NC_000007.13:g.6431654C= , CM000669.1:g.6431654C= GRCh37
NC_000007.12:g.6398179C= NCBI36
NG_029431.1:g.22529C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.395C=
ENST00000704002.1:c.306C= ENSP00000515615.1:p.Pro102=
ENST00000704003.1:c.*160C= ENSP00000515616.1:n.*160C=
ENST00000348035.9:c.207C= MANE Select ENSP00000258737.7:p.Pro69=
ENST00000348035.8:c.207C= ENSP00000258737.7:p.Pro69=
ENST00000356142.4:c.207C= ENSP00000348461.4:p.Pro69=
ENST00000488373.5:n.438C=
ENST00000497741.5:n.223C=
NM_006908.4:c.207C= NP_008839.2:p.Pro69=
NM_018890.3:c.207C= NP_061485.1:p.Pro69=
NM_006908.5:c.207C= MANE Select NP_008839.2:p.Pro69=
NM_018890.4:c.207C= NP_061485.1:p.Pro69=