Canonical Allele Identifier: CA366761313

Gene: RAC1

Linked Data

• ClinVar Variation Id: 1333690
• ClinVar RCV Id: RCV001808906
• dbSNP Id: rs2115201389
• MyVariant Identifiers: chr7:g.6431638A>G (hg19) ; chr7:g.6392007A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392007A>G , CM000669.2:g.6392007A>G	GRCh38
NC_000007.13:g.6431638A>G , CM000669.1:g.6431638A>G	GRCh37
NC_000007.12:g.6398163A>G	NCBI36
NG_029431.1:g.22513A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.379A>G
ENST00000704002.1:c.290A>G	ENSP00000515615.1:p.Tyr97Cys
ENST00000704003.1:c.*144A>G	ENSP00000515616.1:n.*144A>G
ENST00000348035.9:c.191A>G MANE Select	ENSP00000258737.7:p.Tyr64Cys
ENST00000348035.8:c.191A>G	ENSP00000258737.7:p.Tyr64Cys
ENST00000356142.4:c.191A>G	ENSP00000348461.4:p.Tyr64Cys
ENST00000488373.5:n.422A>G
ENST00000497741.5:n.207A>G
NM_006908.4:c.191A>G	NP_008839.2:p.Tyr64Cys
NM_018890.3:c.191A>G	NP_061485.1:p.Tyr64Cys
NM_006908.5:c.191A>G MANE Select	NP_008839.2:p.Tyr64Cys
NM_018890.4:c.191A>G	NP_061485.1:p.Tyr64Cys