Canonical Allele Identifier: CA366760899

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431596C>G (hg19) ; chr7:g.6391965C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391965C>G , CM000669.2:g.6391965C>G	GRCh38
NC_000007.13:g.6431596C>G , CM000669.1:g.6431596C>G	GRCh37
NC_000007.12:g.6398121C>G	NCBI36
NG_029431.1:g.22471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.337C>G
ENST00000704002.1:c.248C>G	ENSP00000515615.1:p.Pro83Arg
ENST00000704003.1:c.*102C>G	ENSP00000515616.1:n.*102C>G
ENST00000348035.9:c.149C>G MANE Select	ENSP00000258737.7:p.Pro50Arg
ENST00000348035.8:c.149C>G	ENSP00000258737.7:p.Pro50Arg
ENST00000356142.4:c.149C>G	ENSP00000348461.4:p.Pro50Arg
ENST00000488373.5:n.380C>G
ENST00000497741.5:n.165C>G
NM_006908.4:c.149C>G	NP_008839.2:p.Pro50Arg
NM_018890.3:c.149C>G	NP_061485.1:p.Pro50Arg
NM_006908.5:c.149C>G MANE Select	NP_008839.2:p.Pro50Arg
NM_018890.4:c.149C>G	NP_061485.1:p.Pro50Arg