Canonical Allele Identifier: CA366760816

Gene: RAC1

Linked Data

• COSMIC: COSM747315 ; COSM1150734
• MyVariant Identifiers: chr7:g.6431584T>G (hg19) ; chr7:g.6391953T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391953T>G , CM000669.2:g.6391953T>G	GRCh38
NC_000007.13:g.6431584T>G , CM000669.1:g.6431584T>G	GRCh37
NC_000007.12:g.6398109T>G	NCBI36
NG_029431.1:g.22459T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.325T>G
ENST00000704002.1:c.236T>G	ENSP00000515615.1:p.Val79Gly
ENST00000704003.1:c.*90T>G	ENSP00000515616.1:n.*90T>G
ENST00000348035.9:c.137T>G MANE Select	ENSP00000258737.7:p.Val46Gly
ENST00000348035.8:c.137T>G	ENSP00000258737.7:p.Val46Gly
ENST00000356142.4:c.137T>G	ENSP00000348461.4:p.Val46Gly
ENST00000488373.5:n.368T>G
ENST00000497741.5:n.153T>G
NM_006908.4:c.137T>G	NP_008839.2:p.Val46Gly
NM_018890.3:c.137T>G	NP_061485.1:p.Val46Gly
NM_006908.5:c.137T>G MANE Select	NP_008839.2:p.Val46Gly
NM_018890.4:c.137T>G	NP_061485.1:p.Val46Gly