Canonical Allele Identifier: CA840972017
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs905296530
gnomAD v4: 7-6392114-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392114A>G , CM000669.2:g.6392114A>G GRCh38
NC_000007.13:g.6431745A>G , CM000669.1:g.6431745A>G GRCh37
NC_000007.12:g.6398270A>G NCBI36
NG_029431.1:g.22620A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.486A>G
ENST00000704002.1:c.324+73A>G ENSP00000515615.1:n.324+73A>G
ENST00000704003.1:c.*178+73A>G ENSP00000515616.1:n.*178+73A>G
ENST00000348035.9:c.225+73A>G MANE Select ENSP00000258737.7:n.225+73A>G
ENST00000348035.8:c.225+73A>G ENSP00000258737.7:n.225+73A>G
ENST00000356142.4:c.225+73A>G ENSP00000348461.4:n.225+73A>G
ENST00000488373.5:n.456+73A>G
ENST00000497741.5:n.241+73A>G
NM_006908.4:c.225+73A>G NP_008839.2:n.225+73A>G
NM_018890.3:c.225+73A>G NP_061485.1:n.225+73A>G
NM_006908.5:c.225+73A>G MANE Select NP_008839.2:n.225+73A>G
NM_018890.4:c.225+73A>G NP_061485.1:n.225+73A>G