Canonical Allele Identifier: CA453648069
Gene: RAC1 HGNC NCBI

Linked Data

gnomAD v4: 7-6391975-G-C
MyVariant Identifiers: chr7:g.6431606G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391975G>C , CM000669.2:g.6391975G>C GRCh38
NC_000007.13:g.6431606G>C , CM000669.1:g.6431606G>C GRCh37
NC_000007.12:g.6398131G>C NCBI36
NG_029431.1:g.22481G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.347G>C
ENST00000704002.1:c.258G>C ENSP00000515615.1:p.Leu86=
ENST00000704003.1:c.*112G>C ENSP00000515616.1:n.*112G>C
ENST00000348035.9:c.159G>C MANE Select ENSP00000258737.7:p.Leu53=
ENST00000348035.8:c.159G>C ENSP00000258737.7:p.Leu53=
ENST00000356142.4:c.159G>C ENSP00000348461.4:p.Leu53=
ENST00000488373.5:n.390G>C
ENST00000497741.5:n.175G>C
NM_006908.4:c.159G>C NP_008839.2:p.Leu53=
NM_018890.3:c.159G>C NP_061485.1:p.Leu53=
NM_006908.5:c.159G>C MANE Select NP_008839.2:p.Leu53=
NM_018890.4:c.159G>C NP_061485.1:p.Leu53=