Canonical Allele Identifier: CA366761235

Gene: RAC1

Linked Data

• ClinVar Variation Id: 1727259
• ClinVar RCV Id: RCV003228809
• MyVariant Identifiers: chr7:g.6431631G>A (hg19) ; chr7:g.6392000G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392000G>A , CM000669.2:g.6392000G>A	GRCh38
NC_000007.13:g.6431631G>A , CM000669.1:g.6431631G>A	GRCh37
NC_000007.12:g.6398156G>A	NCBI36
NG_029431.1:g.22506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.372G>A
ENST00000704002.1:c.283G>A	ENSP00000515615.1:p.Glu95Lys
ENST00000704003.1:c.*137G>A	ENSP00000515616.1:n.*137G>A
ENST00000348035.9:c.184G>A MANE Select	ENSP00000258737.7:p.Glu62Lys
ENST00000348035.8:c.184G>A	ENSP00000258737.7:p.Glu62Lys
ENST00000356142.4:c.184G>A	ENSP00000348461.4:p.Glu62Lys
ENST00000488373.5:n.415G>A
ENST00000497741.5:n.200G>A
NM_006908.4:c.184G>A	NP_008839.2:p.Glu62Lys
NM_018890.3:c.184G>A	NP_061485.1:p.Glu62Lys
NM_006908.5:c.184G>A MANE Select	NP_008839.2:p.Glu62Lys
NM_018890.4:c.184G>A	NP_061485.1:p.Glu62Lys