Canonical Allele Identifier: CA1685476352
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391948T= , CM000669.2:g.6391948T= GRCh38
NC_000007.13:g.6431579T= , CM000669.1:g.6431579T= GRCh37
NC_000007.12:g.6398104T= NCBI36
NG_029431.1:g.22454T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.320T=
ENST00000704002.1:c.231T= ENSP00000515615.1:p.Val77=
ENST00000704003.1:c.*85T= ENSP00000515616.1:n.*85T=
ENST00000348035.9:c.132T= MANE Select ENSP00000258737.7:p.Val44=
ENST00000348035.8:c.132T= ENSP00000258737.7:p.Val44=
ENST00000356142.4:c.132T= ENSP00000348461.4:p.Val44=
ENST00000488373.5:n.363T=
ENST00000497741.5:n.148T=
NM_006908.4:c.132T= NP_008839.2:p.Val44=
NM_018890.3:c.132T= NP_061485.1:p.Val44=
NM_006908.5:c.132T= MANE Select NP_008839.2:p.Val44=
NM_018890.4:c.132T= NP_061485.1:p.Val44=