Canonical Allele Identifier: CA4153656
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs777676140
gnomAD v2: 7-6431657-A-G
gnomAD v4: 7-6392026-A-G
COSMIC: COSM96169

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392026A>G , CM000669.2:g.6392026A>G GRCh38
NC_000007.13:g.6431657A>G , CM000669.1:g.6431657A>G GRCh37
NC_000007.12:g.6398182A>G NCBI36
NG_029431.1:g.22532A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.398A>G
ENST00000704002.1:c.309A>G ENSP00000515615.1:p.Leu103=
ENST00000704003.1:c.*163A>G ENSP00000515616.1:n.*163A>G
ENST00000348035.9:c.210A>G MANE Select ENSP00000258737.7:p.Leu70=
ENST00000348035.8:c.210A>G ENSP00000258737.7:p.Leu70=
ENST00000356142.4:c.210A>G ENSP00000348461.4:p.Leu70=
ENST00000488373.5:n.441A>G
ENST00000497741.5:n.226A>G
NM_006908.4:c.210A>G NP_008839.2:p.Leu70=
NM_018890.3:c.210A>G NP_061485.1:p.Leu70=
NM_006908.5:c.210A>G MANE Select NP_008839.2:p.Leu70=
NM_018890.4:c.210A>G NP_061485.1:p.Leu70=