Canonical Allele Identifier: CA366760736

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431568T>A (hg19) ; chr7:g.6391937T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391937T>A , CM000669.2:g.6391937T>A	GRCh38
NC_000007.13:g.6431568T>A , CM000669.1:g.6431568T>A	GRCh37
NC_000007.12:g.6398093T>A	NCBI36
NG_029431.1:g.22443T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.309T>A
ENST00000704002.1:c.220T>A	ENSP00000515615.1:p.Ser74Thr
ENST00000704003.1:c.*74T>A	ENSP00000515616.1:n.*74T>A
ENST00000348035.9:c.121T>A MANE Select	ENSP00000258737.7:p.Ser41Thr
ENST00000348035.8:c.121T>A	ENSP00000258737.7:p.Ser41Thr
ENST00000356142.4:c.121T>A	ENSP00000348461.4:p.Ser41Thr
ENST00000488373.5:n.352T>A
ENST00000497741.5:n.137T>A
NM_006908.4:c.121T>A	NP_008839.2:p.Ser41Thr
NM_018890.3:c.121T>A	NP_061485.1:p.Ser41Thr
NM_006908.5:c.121T>A MANE Select	NP_008839.2:p.Ser41Thr
NM_018890.4:c.121T>A	NP_061485.1:p.Ser41Thr