Canonical Allele Identifier: CA366760897
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1783104328
gnomAD v3: 7-6391965-C-A
gnomAD v4: 7-6391965-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391965C>A , CM000669.2:g.6391965C>A GRCh38
NC_000007.13:g.6431596C>A , CM000669.1:g.6431596C>A GRCh37
NC_000007.12:g.6398121C>A NCBI36
NG_029431.1:g.22471C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.337C>A
ENST00000704002.1:c.248C>A ENSP00000515615.1:p.Pro83Gln
ENST00000704003.1:c.*102C>A ENSP00000515616.1:n.*102C>A
ENST00000348035.9:c.149C>A MANE Select ENSP00000258737.7:p.Pro50Gln
ENST00000348035.8:c.149C>A ENSP00000258737.7:p.Pro50Gln
ENST00000356142.4:c.149C>A ENSP00000348461.4:p.Pro50Gln
ENST00000488373.5:n.380C>A
ENST00000497741.5:n.165C>A
NM_006908.4:c.149C>A NP_008839.2:p.Pro50Gln
NM_018890.3:c.149C>A NP_061485.1:p.Pro50Gln
NM_006908.5:c.149C>A MANE Select NP_008839.2:p.Pro50Gln
NM_018890.4:c.149C>A NP_061485.1:p.Pro50Gln