Canonical Allele Identifier: CA366760917
Gene: RAC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445284
ClinVar RCV Id: RCV000514583 RCV001821433
dbSNP Id: rs1554263625
MyVariant Identifiers: chr7:g.6431598G>A (hg19) chr7:g.6391967G>A (hg38)
PubMed: PMID:28135719 PMID:28886345
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391967G>A , CM000669.2:g.6391967G>A GRCh38
NC_000007.13:g.6431598G>A , CM000669.1:g.6431598G>A GRCh37
NC_000007.12:g.6398123G>A NCBI36
NG_029431.1:g.22473G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696666.1:n.339G>A
ENST00000704002.1:c.250G>A ENSP00000515615.1:p.Val84Met
ENST00000704003.1:c.*104G>A ENSP00000515616.1:n.*104G>A
ENST00000348035.9:c.151G>A MANE Select ENSP00000258737.7:p.Val51Met
ENST00000348035.8:c.151G>A ENSP00000258737.7:p.Val51Met
ENST00000356142.4:c.151G>A ENSP00000348461.4:p.Val51Met
ENST00000488373.5:n.382G>A
ENST00000497741.5:n.167G>A
NM_006908.4:c.151G>A NP_008839.2:p.Val51Met
NM_018890.3:c.151G>A NP_061485.1:p.Val51Met
NM_006908.5:c.151G>A MANE Select NP_008839.2:p.Val51Met
NM_018890.4:c.151G>A NP_061485.1:p.Val51Met
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