Canonical Allele Identifier: CA366760826

Gene: RAC1

Linked Data

• ClinVar Variation Id: 2505850
• ClinVar RCV Id: RCV003236082
• MyVariant Identifiers: chr7:g.6431587A>G (hg19) ; chr7:g.6391956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391956A>G , CM000669.2:g.6391956A>G	GRCh38
NC_000007.13:g.6431587A>G , CM000669.1:g.6431587A>G	GRCh37
NC_000007.12:g.6398112A>G	NCBI36
NG_029431.1:g.22462A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.328A>G
ENST00000704002.1:c.239A>G	ENSP00000515615.1:p.Asp80Gly
ENST00000704003.1:c.*93A>G	ENSP00000515616.1:n.*93A>G
ENST00000348035.9:c.140A>G MANE Select	ENSP00000258737.7:p.Asp47Gly
ENST00000348035.8:c.140A>G	ENSP00000258737.7:p.Asp47Gly
ENST00000356142.4:c.140A>G	ENSP00000348461.4:p.Asp47Gly
ENST00000488373.5:n.371A>G
ENST00000497741.5:n.156A>G
NM_006908.4:c.140A>G	NP_008839.2:p.Asp47Gly
NM_018890.3:c.140A>G	NP_061485.1:p.Asp47Gly
NM_006908.5:c.140A>G MANE Select	NP_008839.2:p.Asp47Gly
NM_018890.4:c.140A>G	NP_061485.1:p.Asp47Gly