Canonical Allele Identifier: CA16602801
Gene: RAC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376362
ClinVar RCV Id: RCV000421644 RCV000421823 RCV000424053 RCV000432514 RCV000438875
dbSNP Id: rs1057519874
COSMIC: COSM125734 COSM1167878
MyVariant Identifiers: chr7:g.6426892C>T (hg19) chr7:g.6387261C>T (hg38)
CIViC: CA16602801
PubMed: PMID:25056119 PMID:26619011
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6387261C>T , CM000669.2:g.6387261C>T GRCh38
NC_000007.13:g.6426892C>T , CM000669.1:g.6426892C>T GRCh37
NC_000007.12:g.6393417C>T NCBI36
NG_029431.1:g.17767C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696666.1:n.273C>T
ENST00000704002.1:c.85C>T ENSP00000515615.1:p.Pro29Ser
ENST00000704003.1:c.*38C>T ENSP00000515616.1:n.*38C>T
ENST00000348035.9:c.85C>T MANE Select ENSP00000258737.7:p.Pro29Ser
ENST00000348035.8:c.85C>T ENSP00000258737.7:p.Pro29Ser
ENST00000356142.4:c.85C>T ENSP00000348461.4:p.Pro29Ser
ENST00000488373.5:n.316C>T
NM_006908.4:c.85C>T NP_008839.2:p.Pro29Ser
NM_018890.3:c.85C>T NP_061485.1:p.Pro29Ser
NM_006908.5:c.85C>T MANE Select NP_008839.2:p.Pro29Ser
NM_018890.4:c.85C>T NP_061485.1:p.Pro29Ser
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