Canonical Allele Identifier: CA453648092
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431621A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391990A>T , CM000669.2:g.6391990A>T GRCh38
NC_000007.13:g.6431621A>T , CM000669.1:g.6431621A>T GRCh37
NC_000007.12:g.6398146A>T NCBI36
NG_029431.1:g.22496A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.362A>T
ENST00000704002.1:c.273A>T ENSP00000515615.1:p.Thr91=
ENST00000704003.1:c.*127A>T ENSP00000515616.1:n.*127A>T
ENST00000348035.9:c.174A>T MANE Select ENSP00000258737.7:p.Thr58=
ENST00000348035.8:c.174A>T ENSP00000258737.7:p.Thr58=
ENST00000356142.4:c.174A>T ENSP00000348461.4:p.Thr58=
ENST00000488373.5:n.405A>T
ENST00000497741.5:n.190A>T
NM_006908.4:c.174A>T NP_008839.2:p.Thr58=
NM_018890.3:c.174A>T NP_061485.1:p.Thr58=
NM_006908.5:c.174A>T MANE Select NP_008839.2:p.Thr58=
NM_018890.4:c.174A>T NP_061485.1:p.Thr58=