Canonical Allele Identifier: CA4153643
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs763293034
gnomAD v2: 7-6431528-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391897A>G , CM000669.2:g.6391897A>G GRCh38
NC_000007.13:g.6431528A>G , CM000669.1:g.6431528A>G GRCh37
NC_000007.12:g.6398053A>G NCBI36
NG_029431.1:g.22403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.296-27A>G
ENST00000704002.1:c.207-27A>G ENSP00000515615.1:n.207-27A>G
ENST00000704003.1:c.*61-27A>G ENSP00000515616.1:n.*61-27A>G
ENST00000348035.9:c.108-27A>G MANE Select ENSP00000258737.7:n.108-27A>G
ENST00000348035.8:c.108-27A>G ENSP00000258737.7:n.108-27A>G
ENST00000356142.4:c.108-27A>G ENSP00000348461.4:n.108-27A>G
ENST00000488373.5:n.339-27A>G
ENST00000497741.5:n.124-27A>G
NM_006908.4:c.108-27A>G NP_008839.2:n.108-27A>G
NM_018890.3:c.108-27A>G NP_061485.1:n.108-27A>G
NM_006908.5:c.108-27A>G MANE Select NP_008839.2:n.108-27A>G
NM_018890.4:c.108-27A>G NP_061485.1:n.108-27A>G