Canonical Allele Identifier: CA1685476530

Gene: RAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392071_6392072delinsCT , CM000669.2:g.6392071_6392072delinsCT	GRCh38
NC_000007.13:g.6431702_6431703delinsCT , CM000669.1:g.6431702_6431703delinsCT	GRCh37
NC_000007.12:g.6398227_6398228delinsCT	NCBI36
NG_029431.1:g.22577_22578delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.443_444delinsCT
ENST00000704002.1:c.324+30_324+31delinsCT	ENSP00000515615.1:n.324+30_324+31delinsCT
ENST00000704003.1:c.*178+30_*178+31delinsCT	ENSP00000515616.1:n.*178+30_*178+31delinsCT
ENST00000348035.9:c.225+30_225+31delinsCT MANE Select	ENSP00000258737.7:n.225+30_225+31delinsCT
ENST00000348035.8:c.225+30_225+31delinsCT	ENSP00000258737.7:n.225+30_225+31delinsCT
ENST00000356142.4:c.225+30_225+31delinsCT	ENSP00000348461.4:n.225+30_225+31delinsCT
ENST00000488373.5:n.456+30_456+31delinsCT
ENST00000497741.5:n.241+30_241+31delinsCT
NM_006908.4:c.225+30_225+31delinsCT	NP_008839.2:n.225+30_225+31delinsCT
NM_018890.3:c.225+30_225+31delinsCT	NP_061485.1:n.225+30_225+31delinsCT
NM_006908.5:c.225+30_225+31delinsCT MANE Select	NP_008839.2:n.225+30_225+31delinsCT
NM_018890.4:c.225+30_225+31delinsCT	NP_061485.1:n.225+30_225+31delinsCT