Canonical Allele Identifier: CA366761277
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1459952760
gnomAD v2: 7-6431635-A-T
gnomAD v4: 7-6392004-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392004A>T , CM000669.2:g.6392004A>T GRCh38
NC_000007.13:g.6431635A>T , CM000669.1:g.6431635A>T GRCh37
NC_000007.12:g.6398160A>T NCBI36
NG_029431.1:g.22510A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.376A>T
ENST00000704002.1:c.287A>T ENSP00000515615.1:p.Asp96Val
ENST00000704003.1:c.*141A>T ENSP00000515616.1:n.*141A>T
ENST00000348035.9:c.188A>T MANE Select ENSP00000258737.7:p.Asp63Val
ENST00000348035.8:c.188A>T ENSP00000258737.7:p.Asp63Val
ENST00000356142.4:c.188A>T ENSP00000348461.4:p.Asp63Val
ENST00000488373.5:n.419A>T
ENST00000497741.5:n.204A>T
NM_006908.4:c.188A>T NP_008839.2:p.Asp63Val
NM_018890.3:c.188A>T NP_061485.1:p.Asp63Val
NM_006908.5:c.188A>T MANE Select NP_008839.2:p.Asp63Val
NM_018890.4:c.188A>T NP_061485.1:p.Asp63Val