Canonical Allele Identifier: CA4153641

Gene: RAC1

Linked Data

• dbSNP Id: rs553485430
• ExAC: 7:6431523 C / CT
• gnomAD v2: 7-6431523-C-CT
• gnomAD v3: 7-6391892-C-CT
• gnomAD v4: 7-6391892-C-CT
• MyVariant Identifiers: chr7:g.6431523_6431524insT (hg19) ; chr7:g.6391892_6391893insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391893dup , CM000669.2:g.6391893dup	GRCh38
NC_000007.13:g.6431524dup , CM000669.1:g.6431524dup	GRCh37
NC_000007.12:g.6398049dup	NCBI36
NG_029431.1:g.22399dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.296-31dup
ENST00000704002.1:c.207-31dup	ENSP00000515615.1:n.207-31dup
ENST00000704003.1:c.*61-31dup	ENSP00000515616.1:n.*61-31dup
ENST00000348035.9:c.108-31dup MANE Select	ENSP00000258737.7:n.108-31dup
ENST00000348035.8:c.108-31dup	ENSP00000258737.7:n.108-31dup
ENST00000356142.4:c.108-31dup	ENSP00000348461.4:n.108-31dup
ENST00000488373.5:n.339-31dup
ENST00000497741.5:n.124-31dup
NM_006908.4:c.108-31dup	NP_008839.2:n.108-31dup
NM_018890.3:c.108-31dup	NP_061485.1:n.108-31dup
NM_006908.5:c.108-31dup MANE Select	NP_008839.2:n.108-31dup
NM_018890.4:c.108-31dup	NP_061485.1:n.108-31dup