Canonical Allele Identifier: CA4153640

Gene: RAC1

Linked Data

• dbSNP Id: rs769952086
• ExAC: 7:6431515 T / C
• gnomAD v2: 7-6431515-T-C
• gnomAD v3: 7-6391884-T-C
• gnomAD v4: 7-6391884-T-C
• MyVariant Identifiers: chr7:g.6431515T>C (hg19) ; chr7:g.6391884T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391884T>C , CM000669.2:g.6391884T>C	GRCh38
NC_000007.13:g.6431515T>C , CM000669.1:g.6431515T>C	GRCh37
NC_000007.12:g.6398040T>C	NCBI36
NG_029431.1:g.22390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.296-40T>C
ENST00000704002.1:c.207-40T>C	ENSP00000515615.1:n.207-40T>C
ENST00000704003.1:c.*61-40T>C	ENSP00000515616.1:n.*61-40T>C
ENST00000348035.9:c.108-40T>C MANE Select	ENSP00000258737.7:n.108-40T>C
ENST00000348035.8:c.108-40T>C	ENSP00000258737.7:n.108-40T>C
ENST00000356142.4:c.108-40T>C	ENSP00000348461.4:n.108-40T>C
ENST00000488373.5:n.339-40T>C
ENST00000497741.5:n.124-40T>C
NM_006908.4:c.108-40T>C	NP_008839.2:n.108-40T>C
NM_018890.3:c.108-40T>C	NP_061485.1:n.108-40T>C
NM_006908.5:c.108-40T>C MANE Select	NP_008839.2:n.108-40T>C
NM_018890.4:c.108-40T>C	NP_061485.1:n.108-40T>C