Canonical Allele Identifier: CA366761378

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431644G>C (hg19) ; chr7:g.6392013G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392013G>C , CM000669.2:g.6392013G>C	GRCh38
NC_000007.13:g.6431644G>C , CM000669.1:g.6431644G>C	GRCh37
NC_000007.12:g.6398169G>C	NCBI36
NG_029431.1:g.22519G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.385G>C
ENST00000704002.1:c.296G>C	ENSP00000515615.1:p.Arg99Thr
ENST00000704003.1:c.*150G>C	ENSP00000515616.1:n.*150G>C
ENST00000348035.9:c.197G>C MANE Select	ENSP00000258737.7:p.Arg66Thr
ENST00000348035.8:c.197G>C	ENSP00000258737.7:p.Arg66Thr
ENST00000356142.4:c.197G>C	ENSP00000348461.4:p.Arg66Thr
ENST00000488373.5:n.428G>C
ENST00000497741.5:n.213G>C
NM_006908.4:c.197G>C	NP_008839.2:p.Arg66Thr
NM_018890.3:c.197G>C	NP_061485.1:p.Arg66Thr
NM_006908.5:c.197G>C MANE Select	NP_008839.2:p.Arg66Thr
NM_018890.4:c.197G>C	NP_061485.1:p.Arg66Thr