Canonical Allele Identifier: CA2681706085
Gene: RAC1 HGNC NCBI

Linked Data

gnomAD v4: 7-6392059-CT-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392063del , CM000669.2:g.6392063del GRCh38
NC_000007.13:g.6431694del , CM000669.1:g.6431694del GRCh37
NC_000007.12:g.6398219del NCBI36
NG_029431.1:g.22569del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.435del
ENST00000704002.1:c.324+22del ENSP00000515615.1:n.324+22del
ENST00000704003.1:c.*178+22del ENSP00000515616.1:n.*178+22del
ENST00000348035.9:c.225+22del MANE Select ENSP00000258737.7:n.225+22del
ENST00000348035.8:c.225+22del ENSP00000258737.7:n.225+22del
ENST00000356142.4:c.225+22del ENSP00000348461.4:n.225+22del
ENST00000488373.5:n.456+22del
ENST00000497741.5:n.241+22del
NM_006908.4:c.225+22del NP_008839.2:n.225+22del
NM_018890.3:c.225+22del NP_061485.1:n.225+22del
NM_006908.5:c.225+22del MANE Select NP_008839.2:n.225+22del
NM_018890.4:c.225+22del NP_061485.1:n.225+22del