Canonical Allele Identifier: CA366761068

Gene: RAC1

Linked Data

• ClinVar Variation Id: 2413045
• ClinVar RCV Id: RCV003110060
• dbSNP Id: rs2115201346
• MyVariant Identifiers: chr7:g.6431614G>T (hg19) ; chr7:g.6391983G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391983G>T , CM000669.2:g.6391983G>T	GRCh38
NC_000007.13:g.6431614G>T , CM000669.1:g.6431614G>T	GRCh37
NC_000007.12:g.6398139G>T	NCBI36
NG_029431.1:g.22489G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.355G>T
ENST00000704002.1:c.266G>T	ENSP00000515615.1:p.Trp89Leu
ENST00000704003.1:c.*120G>T	ENSP00000515616.1:n.*120G>T
ENST00000348035.9:c.167G>T MANE Select	ENSP00000258737.7:p.Trp56Leu
ENST00000348035.8:c.167G>T	ENSP00000258737.7:p.Trp56Leu
ENST00000356142.4:c.167G>T	ENSP00000348461.4:p.Trp56Leu
ENST00000488373.5:n.398G>T
ENST00000497741.5:n.183G>T
NM_006908.4:c.167G>T	NP_008839.2:p.Trp56Leu
NM_018890.3:c.167G>T	NP_061485.1:p.Trp56Leu
NM_006908.5:c.167G>T MANE Select	NP_008839.2:p.Trp56Leu
NM_018890.4:c.167G>T	NP_061485.1:p.Trp56Leu