Canonical Allele Identifier: CA1098031759
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1783107422
gnomAD v3: 7-6392099-T-TA
gnomAD v4: 7-6392099-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392101dup , CM000669.2:g.6392101dup GRCh38
NC_000007.13:g.6431732dup , CM000669.1:g.6431732dup GRCh37
NC_000007.12:g.6398257dup NCBI36
NG_029431.1:g.22607dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.473dup
ENST00000704002.1:c.324+60dup ENSP00000515615.1:n.324+60dup
ENST00000704003.1:c.*178+60dup ENSP00000515616.1:n.*178+60dup
ENST00000348035.9:c.225+60dup MANE Select ENSP00000258737.7:n.225+60dup
ENST00000348035.8:c.225+60dup ENSP00000258737.7:n.225+60dup
ENST00000356142.4:c.225+60dup ENSP00000348461.4:n.225+60dup
ENST00000488373.5:n.456+60dup
ENST00000497741.5:n.241+60dup
NM_006908.4:c.225+60dup NP_008839.2:n.225+60dup
NM_018890.3:c.225+60dup NP_061485.1:n.225+60dup
NM_006908.5:c.225+60dup MANE Select NP_008839.2:n.225+60dup
NM_018890.4:c.225+60dup NP_061485.1:n.225+60dup