Canonical Allele Identifier: CA572592364

Gene: RAC1

Linked Data

• dbSNP Id: rs1444251124
• gnomAD v2: 7-6431857-T-A
• gnomAD v3: 7-6392226-T-A
• gnomAD v4: 7-6392226-T-A
• MyVariant Identifiers: chr7:g.6431857T>A (hg19) ; chr7:g.6392226T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392226T>A , CM000669.2:g.6392226T>A	GRCh38
NC_000007.13:g.6431857T>A , CM000669.1:g.6431857T>A	GRCh37
NC_000007.12:g.6398382T>A	NCBI36
NG_029431.1:g.22732T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.598T>A
ENST00000704002.1:c.324+185T>A	ENSP00000515615.1:n.324+185T>A
ENST00000704003.1:c.*178+185T>A	ENSP00000515616.1:n.*178+185T>A
ENST00000348035.9:c.225+185T>A MANE Select	ENSP00000258737.7:n.225+185T>A
ENST00000348035.8:c.225+185T>A	ENSP00000258737.7:n.225+185T>A
ENST00000356142.4:c.225+185T>A	ENSP00000348461.4:n.225+185T>A
ENST00000488373.5:n.456+185T>A
ENST00000497741.5:n.241+185T>A
NM_006908.4:c.225+185T>A	NP_008839.2:n.225+185T>A
NM_018890.3:c.225+185T>A	NP_061485.1:n.225+185T>A
NM_006908.5:c.225+185T>A MANE Select	NP_008839.2:n.225+185T>A
NM_018890.4:c.225+185T>A	NP_061485.1:n.225+185T>A