Canonical Allele Identifier: CA453648022
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431570T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391939T>A , CM000669.2:g.6391939T>A GRCh38
NC_000007.13:g.6431570T>A , CM000669.1:g.6431570T>A GRCh37
NC_000007.12:g.6398095T>A NCBI36
NG_029431.1:g.22445T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.311T>A
ENST00000704002.1:c.222T>A ENSP00000515615.1:p.Ser74=
ENST00000704003.1:c.*76T>A ENSP00000515616.1:n.*76T>A
ENST00000348035.9:c.123T>A MANE Select ENSP00000258737.7:p.Ser41=
ENST00000348035.8:c.123T>A ENSP00000258737.7:p.Ser41=
ENST00000356142.4:c.123T>A ENSP00000348461.4:p.Ser41=
ENST00000488373.5:n.354T>A
ENST00000497741.5:n.139T>A
NM_006908.4:c.123T>A NP_008839.2:p.Ser41=
NM_018890.3:c.123T>A NP_061485.1:p.Ser41=
NM_006908.5:c.123T>A MANE Select NP_008839.2:p.Ser41=
NM_018890.4:c.123T>A NP_061485.1:p.Ser41=