Canonical Allele Identifier: CA453648028
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431573C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391942C>T , CM000669.2:g.6391942C>T GRCh38
NC_000007.13:g.6431573C>T , CM000669.1:g.6431573C>T GRCh37
NC_000007.12:g.6398098C>T NCBI36
NG_029431.1:g.22448C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.314C>T
ENST00000704002.1:c.225C>T ENSP00000515615.1:p.Ala75=
ENST00000704003.1:c.*79C>T ENSP00000515616.1:n.*79C>T
ENST00000348035.9:c.126C>T MANE Select ENSP00000258737.7:p.Ala42=
ENST00000348035.8:c.126C>T ENSP00000258737.7:p.Ala42=
ENST00000356142.4:c.126C>T ENSP00000348461.4:p.Ala42=
ENST00000488373.5:n.357C>T
ENST00000497741.5:n.142C>T
NM_006908.4:c.126C>T NP_008839.2:p.Ala42=
NM_018890.3:c.126C>T NP_061485.1:p.Ala42=
NM_006908.5:c.126C>T MANE Select NP_008839.2:p.Ala42=
NM_018890.4:c.126C>T NP_061485.1:p.Ala42=