Canonical Allele Identifier: CA1685476489
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392058A= , CM000669.2:g.6392058A= GRCh38
NC_000007.13:g.6431689A= , CM000669.1:g.6431689A= GRCh37
NC_000007.12:g.6398214A= NCBI36
NG_029431.1:g.22564A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.430A=
ENST00000704002.1:c.324+17A= ENSP00000515615.1:n.324+17A=
ENST00000704003.1:c.*178+17A= ENSP00000515616.1:n.*178+17A=
ENST00000348035.9:c.225+17A= MANE Select ENSP00000258737.7:n.225+17A=
ENST00000348035.8:c.225+17A= ENSP00000258737.7:n.225+17A=
ENST00000356142.4:c.225+17A= ENSP00000348461.4:n.225+17A=
ENST00000488373.5:n.456+17A=
ENST00000497741.5:n.241+17A=
NM_006908.4:c.225+17A= NP_008839.2:n.225+17A=
NM_018890.3:c.225+17A= NP_061485.1:n.225+17A=
NM_006908.5:c.225+17A= MANE Select NP_008839.2:n.225+17A=
NM_018890.4:c.225+17A= NP_061485.1:n.225+17A=