Canonical Allele Identifier: CA1685476652
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392113T= , CM000669.2:g.6392113T= GRCh38
NC_000007.13:g.6431744T= , CM000669.1:g.6431744T= GRCh37
NC_000007.12:g.6398269T= NCBI36
NG_029431.1:g.22619T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.485T=
ENST00000704002.1:c.324+72T= ENSP00000515615.1:n.324+72T=
ENST00000704003.1:c.*178+72T= ENSP00000515616.1:n.*178+72T=
ENST00000348035.9:c.225+72T= MANE Select ENSP00000258737.7:n.225+72T=
ENST00000348035.8:c.225+72T= ENSP00000258737.7:n.225+72T=
ENST00000356142.4:c.225+72T= ENSP00000348461.4:n.225+72T=
ENST00000488373.5:n.456+72T=
ENST00000497741.5:n.241+72T=
NM_006908.4:c.225+72T= NP_008839.2:n.225+72T=
NM_018890.3:c.225+72T= NP_061485.1:n.225+72T=
NM_006908.5:c.225+72T= MANE Select NP_008839.2:n.225+72T=
NM_018890.4:c.225+72T= NP_061485.1:n.225+72T=