Canonical Allele Identifier: CA453648014
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1304409388
gnomAD v2: 7-6431555-C-G
gnomAD v4: 7-6391924-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391924C>G , CM000669.2:g.6391924C>G GRCh38
NC_000007.13:g.6431555C>G , CM000669.1:g.6431555C>G GRCh37
NC_000007.12:g.6398080C>G NCBI36
NG_029431.1:g.22430C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.296C>G
ENST00000704002.1:c.207C>G ENSP00000515615.1:p.Ser69Arg
ENST00000704003.1:c.*61C>G ENSP00000515616.1:n.*61C>G
ENST00000348035.9:c.108C>G MANE Select ENSP00000258737.7:p.Val36=
ENST00000348035.8:c.108C>G ENSP00000258737.7:p.Val36=
ENST00000356142.4:c.108C>G ENSP00000348461.4:p.Val36=
ENST00000488373.5:n.339C>G
ENST00000497741.5:n.124C>G
NM_006908.4:c.108C>G NP_008839.2:p.Val36=
NM_018890.3:c.108C>G NP_061485.1:p.Val36=
NM_006908.5:c.108C>G MANE Select NP_008839.2:p.Val36=
NM_018890.4:c.108C>G NP_061485.1:p.Val36=