Canonical Allele Identifier: CA366760819

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431586G>A (hg19) ; chr7:g.6391955G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391955G>A , CM000669.2:g.6391955G>A	GRCh38
NC_000007.13:g.6431586G>A , CM000669.1:g.6431586G>A	GRCh37
NC_000007.12:g.6398111G>A	NCBI36
NG_029431.1:g.22461G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.327G>A
ENST00000704002.1:c.238G>A	ENSP00000515615.1:p.Asp80Asn
ENST00000704003.1:c.*92G>A	ENSP00000515616.1:n.*92G>A
ENST00000348035.9:c.139G>A MANE Select	ENSP00000258737.7:p.Asp47Asn
ENST00000348035.8:c.139G>A	ENSP00000258737.7:p.Asp47Asn
ENST00000356142.4:c.139G>A	ENSP00000348461.4:p.Asp47Asn
ENST00000488373.5:n.370G>A
ENST00000497741.5:n.155G>A
NM_006908.4:c.139G>A	NP_008839.2:p.Asp47Asn
NM_018890.3:c.139G>A	NP_061485.1:p.Asp47Asn
NM_006908.5:c.139G>A MANE Select	NP_008839.2:p.Asp47Asn
NM_018890.4:c.139G>A	NP_061485.1:p.Asp47Asn