Canonical Allele Identifier: CA4153645

Gene: RAC1

Linked Data

• dbSNP Id: rs376284529
• ExAC: 7:6431529 C / G
• gnomAD v2: 7-6431529-C-G
• gnomAD v4: 7-6391898-C-G
• MyVariant Identifiers: chr7:g.6431529C>G (hg19) ; chr7:g.6391898C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391898C>G , CM000669.2:g.6391898C>G	GRCh38
NC_000007.13:g.6431529C>G , CM000669.1:g.6431529C>G	GRCh37
NC_000007.12:g.6398054C>G	NCBI36
NG_029431.1:g.22404C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.296-26C>G
ENST00000704002.1:c.207-26C>G	ENSP00000515615.1:n.207-26C>G
ENST00000704003.1:c.*61-26C>G	ENSP00000515616.1:n.*61-26C>G
ENST00000348035.9:c.108-26C>G MANE Select	ENSP00000258737.7:n.108-26C>G
ENST00000348035.8:c.108-26C>G	ENSP00000258737.7:n.108-26C>G
ENST00000356142.4:c.108-26C>G	ENSP00000348461.4:n.108-26C>G
ENST00000488373.5:n.339-26C>G
ENST00000497741.5:n.124-26C>G
NM_006908.4:c.108-26C>G	NP_008839.2:n.108-26C>G
NM_018890.3:c.108-26C>G	NP_061485.1:n.108-26C>G
NM_006908.5:c.108-26C>G MANE Select	NP_008839.2:n.108-26C>G
NM_018890.4:c.108-26C>G	NP_061485.1:n.108-26C>G