Canonical Allele Identifier: CA366761081

Gene: RAC1

Linked Data

• ClinVar Variation Id: 1027690
• ClinVar RCV Id: RCV001328553
• dbSNP Id: rs1783105049
• MyVariant Identifiers: chr7:g.6431615G>C (hg19) ; chr7:g.6391984G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391984G>C , CM000669.2:g.6391984G>C	GRCh38
NC_000007.13:g.6431615G>C , CM000669.1:g.6431615G>C	GRCh37
NC_000007.12:g.6398140G>C	NCBI36
NG_029431.1:g.22490G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.356G>C
ENST00000704002.1:c.267G>C	ENSP00000515615.1:p.Trp89Cys
ENST00000704003.1:c.*121G>C	ENSP00000515616.1:n.*121G>C
ENST00000348035.9:c.168G>C MANE Select	ENSP00000258737.7:p.Trp56Cys
ENST00000348035.8:c.168G>C	ENSP00000258737.7:p.Trp56Cys
ENST00000356142.4:c.168G>C	ENSP00000348461.4:p.Trp56Cys
ENST00000488373.5:n.399G>C
ENST00000497741.5:n.184G>C
NM_006908.4:c.168G>C	NP_008839.2:p.Trp56Cys
NM_018890.3:c.168G>C	NP_061485.1:p.Trp56Cys
NM_006908.5:c.168G>C MANE Select	NP_008839.2:p.Trp56Cys
NM_018890.4:c.168G>C	NP_061485.1:p.Trp56Cys