Canonical Allele Identifier: CA453648322
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431657A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392026A>T , CM000669.2:g.6392026A>T GRCh38
NC_000007.13:g.6431657A>T , CM000669.1:g.6431657A>T GRCh37
NC_000007.12:g.6398182A>T NCBI36
NG_029431.1:g.22532A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.398A>T
ENST00000704002.1:c.309A>T ENSP00000515615.1:p.Leu103=
ENST00000704003.1:c.*163A>T ENSP00000515616.1:n.*163A>T
ENST00000348035.9:c.210A>T MANE Select ENSP00000258737.7:p.Leu70=
ENST00000348035.8:c.210A>T ENSP00000258737.7:p.Leu70=
ENST00000356142.4:c.210A>T ENSP00000348461.4:p.Leu70=
ENST00000488373.5:n.441A>T
ENST00000497741.5:n.226A>T
NM_006908.4:c.210A>T NP_008839.2:p.Leu70=
NM_018890.3:c.210A>T NP_061485.1:p.Leu70=
NM_006908.5:c.210A>T MANE Select NP_008839.2:p.Leu70=
NM_018890.4:c.210A>T NP_061485.1:p.Leu70=