Canonical Allele Identifier: CA366761505
Gene: RAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392022C>A , CM000669.2:g.6392022C>A GRCh38
NC_000007.13:g.6431653C>A , CM000669.1:g.6431653C>A GRCh37
NC_000007.12:g.6398178C>A NCBI36
NG_029431.1:g.22528C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.394C>A
ENST00000704002.1:c.305C>A ENSP00000515615.1:p.Pro102His
ENST00000704003.1:c.*159C>A ENSP00000515616.1:n.*159C>A
ENST00000348035.9:c.206C>A MANE Select ENSP00000258737.7:p.Pro69His
ENST00000348035.8:c.206C>A ENSP00000258737.7:p.Pro69His
ENST00000356142.4:c.206C>A ENSP00000348461.4:p.Pro69His
ENST00000488373.5:n.437C>A
ENST00000497741.5:n.222C>A
NM_006908.4:c.206C>A NP_008839.2:p.Pro69His
NM_018890.3:c.206C>A NP_061485.1:p.Pro69His
NM_006908.5:c.206C>A MANE Select NP_008839.2:p.Pro69His
NM_018890.4:c.206C>A NP_061485.1:p.Pro69His