Canonical Allele Identifier: CA453648038
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431585A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391954A>T , CM000669.2:g.6391954A>T GRCh38
NC_000007.13:g.6431585A>T , CM000669.1:g.6431585A>T GRCh37
NC_000007.12:g.6398110A>T NCBI36
NG_029431.1:g.22460A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.326A>T
ENST00000704002.1:c.237A>T ENSP00000515615.1:p.Val79=
ENST00000704003.1:c.*91A>T ENSP00000515616.1:n.*91A>T
ENST00000348035.9:c.138A>T MANE Select ENSP00000258737.7:p.Val46=
ENST00000348035.8:c.138A>T ENSP00000258737.7:p.Val46=
ENST00000356142.4:c.138A>T ENSP00000348461.4:p.Val46=
ENST00000488373.5:n.369A>T
ENST00000497741.5:n.154A>T
NM_006908.4:c.138A>T NP_008839.2:p.Val46=
NM_018890.3:c.138A>T NP_061485.1:p.Val46=
NM_006908.5:c.138A>T MANE Select NP_008839.2:p.Val46=
NM_018890.4:c.138A>T NP_061485.1:p.Val46=