Canonical Allele Identifier: CA1098031729
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1783105946
gnomAD v3: 7-6392058-A-AT
gnomAD v4: 7-6392058-A-AT

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392058_6392059insT , CM000669.2:g.6392058_6392059insT GRCh38
NC_000007.13:g.6431689_6431690insT , CM000669.1:g.6431689_6431690insT GRCh37
NC_000007.12:g.6398214_6398215insT NCBI36
NG_029431.1:g.22564_22565insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.430_431insT
ENST00000704002.1:c.324+17_324+18insT ENSP00000515615.1:n.324+17_324+18insT
ENST00000704003.1:c.*178+17_*178+18insT ENSP00000515616.1:n.*178+17_*178+18insT
ENST00000348035.9:c.225+17_225+18insT MANE Select ENSP00000258737.7:n.225+17_225+18insT
ENST00000348035.8:c.225+17_225+18insT ENSP00000258737.7:n.225+17_225+18insT
ENST00000356142.4:c.225+17_225+18insT ENSP00000348461.4:n.225+17_225+18insT
ENST00000488373.5:n.456+17_456+18insT
ENST00000497741.5:n.241+17_241+18insT
NM_006908.4:c.225+17_225+18insT NP_008839.2:n.225+17_225+18insT
NM_018890.3:c.225+17_225+18insT NP_061485.1:n.225+17_225+18insT
NM_006908.5:c.225+17_225+18insT MANE Select NP_008839.2:n.225+17_225+18insT
NM_018890.4:c.225+17_225+18insT NP_061485.1:n.225+17_225+18insT