Canonical Allele Identifier: CA453648047
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431591A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391960A>G , CM000669.2:g.6391960A>G GRCh38
NC_000007.13:g.6431591A>G , CM000669.1:g.6431591A>G GRCh37
NC_000007.12:g.6398116A>G NCBI36
NG_029431.1:g.22466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.332A>G
ENST00000704002.1:c.243A>G ENSP00000515615.1:p.Gly81=
ENST00000704003.1:c.*97A>G ENSP00000515616.1:n.*97A>G
ENST00000348035.9:c.144A>G MANE Select ENSP00000258737.7:p.Gly48=
ENST00000348035.8:c.144A>G ENSP00000258737.7:p.Gly48=
ENST00000356142.4:c.144A>G ENSP00000348461.4:p.Gly48=
ENST00000488373.5:n.375A>G
ENST00000497741.5:n.160A>G
NM_006908.4:c.144A>G NP_008839.2:p.Gly48=
NM_018890.3:c.144A>G NP_061485.1:p.Gly48=
NM_006908.5:c.144A>G MANE Select NP_008839.2:p.Gly48=
NM_018890.4:c.144A>G NP_061485.1:p.Gly48=