Canonical Allele Identifier: CA366761132
Gene: RAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391988A>C , CM000669.2:g.6391988A>C GRCh38
NC_000007.13:g.6431619A>C , CM000669.1:g.6431619A>C GRCh37
NC_000007.12:g.6398144A>C NCBI36
NG_029431.1:g.22494A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.360A>C
ENST00000704002.1:c.271A>C ENSP00000515615.1:p.Thr91Pro
ENST00000704003.1:c.*125A>C ENSP00000515616.1:n.*125A>C
ENST00000348035.9:c.172A>C MANE Select ENSP00000258737.7:p.Thr58Pro
ENST00000348035.8:c.172A>C ENSP00000258737.7:p.Thr58Pro
ENST00000356142.4:c.172A>C ENSP00000348461.4:p.Thr58Pro
ENST00000488373.5:n.403A>C
ENST00000497741.5:n.188A>C
NM_006908.4:c.172A>C NP_008839.2:p.Thr58Pro
NM_018890.3:c.172A>C NP_061485.1:p.Thr58Pro
NM_006908.5:c.172A>C MANE Select NP_008839.2:p.Thr58Pro
NM_018890.4:c.172A>C NP_061485.1:p.Thr58Pro