Canonical Allele Identifier: CA1685476847
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1783109051

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392201G>C , CM000669.2:g.6392201G>C GRCh38
NC_000007.13:g.6431832G>C , CM000669.1:g.6431832G>C GRCh37
NC_000007.12:g.6398357G>C NCBI36
NG_029431.1:g.22707G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.573G>C
ENST00000704002.1:c.324+160G>C ENSP00000515615.1:n.324+160G>C
ENST00000704003.1:c.*178+160G>C ENSP00000515616.1:n.*178+160G>C
ENST00000348035.9:c.225+160G>C MANE Select ENSP00000258737.7:n.225+160G>C
ENST00000348035.8:c.225+160G>C ENSP00000258737.7:n.225+160G>C
ENST00000356142.4:c.225+160G>C ENSP00000348461.4:n.225+160G>C
ENST00000488373.5:n.456+160G>C
ENST00000497741.5:n.241+160G>C
NM_006908.4:c.225+160G>C NP_008839.2:n.225+160G>C
NM_018890.3:c.225+160G>C NP_061485.1:n.225+160G>C
NM_006908.5:c.225+160G>C MANE Select NP_008839.2:n.225+160G>C
NM_018890.4:c.225+160G>C NP_061485.1:n.225+160G>C