Canonical Allele Identifier: CA453648098
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431624T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391993T>A , CM000669.2:g.6391993T>A GRCh38
NC_000007.13:g.6431624T>A , CM000669.1:g.6431624T>A GRCh37
NC_000007.12:g.6398149T>A NCBI36
NG_029431.1:g.22499T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.365T>A
ENST00000704002.1:c.276T>A ENSP00000515615.1:p.Ala92=
ENST00000704003.1:c.*130T>A ENSP00000515616.1:n.*130T>A
ENST00000348035.9:c.177T>A MANE Select ENSP00000258737.7:p.Ala59=
ENST00000348035.8:c.177T>A ENSP00000258737.7:p.Ala59=
ENST00000356142.4:c.177T>A ENSP00000348461.4:p.Ala59=
ENST00000488373.5:n.408T>A
ENST00000497741.5:n.193T>A
NM_006908.4:c.177T>A NP_008839.2:p.Ala59=
NM_018890.3:c.177T>A NP_061485.1:p.Ala59=
NM_006908.5:c.177T>A MANE Select NP_008839.2:p.Ala59=
NM_018890.4:c.177T>A NP_061485.1:p.Ala59=