Canonical Allele Identifier: CA366760688

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431557T>G (hg19) ; chr7:g.6391926T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391926T>G , CM000669.2:g.6391926T>G	GRCh38
NC_000007.13:g.6431557T>G , CM000669.1:g.6431557T>G	GRCh37
NC_000007.12:g.6398082T>G	NCBI36
NG_029431.1:g.22432T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.298T>G
ENST00000704002.1:c.209T>G	ENSP00000515615.1:p.Phe70Cys
ENST00000704003.1:c.*63T>G	ENSP00000515616.1:n.*63T>G
ENST00000348035.9:c.110T>G MANE Select	ENSP00000258737.7:p.Phe37Cys
ENST00000348035.8:c.110T>G	ENSP00000258737.7:p.Phe37Cys
ENST00000356142.4:c.110T>G	ENSP00000348461.4:p.Phe37Cys
ENST00000488373.5:n.341T>G
ENST00000497741.5:n.126T>G
NM_006908.4:c.110T>G	NP_008839.2:p.Phe37Cys
NM_018890.3:c.110T>G	NP_061485.1:p.Phe37Cys
NM_006908.5:c.110T>G MANE Select	NP_008839.2:p.Phe37Cys
NM_018890.4:c.110T>G	NP_061485.1:p.Phe37Cys