Canonical Allele Identifier: CA453648337

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431660C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392029C>G , CM000669.2:g.6392029C>G	GRCh38
NC_000007.13:g.6431660C>G , CM000669.1:g.6431660C>G	GRCh37
NC_000007.12:g.6398185C>G	NCBI36
NG_029431.1:g.22535C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.401C>G
ENST00000704002.1:c.312C>G	ENSP00000515615.1:p.Ser104=
ENST00000704003.1:c.*166C>G	ENSP00000515616.1:n.*166C>G
ENST00000348035.9:c.213C>G MANE Select	ENSP00000258737.7:p.Ser71=
ENST00000348035.8:c.213C>G	ENSP00000258737.7:p.Ser71=
ENST00000356142.4:c.213C>G	ENSP00000348461.4:p.Ser71=
ENST00000488373.5:n.444C>G
ENST00000497741.5:n.229C>G
NM_006908.4:c.213C>G	NP_008839.2:p.Ser71=
NM_018890.3:c.213C>G	NP_061485.1:p.Ser71=
NM_006908.5:c.213C>G MANE Select	NP_008839.2:p.Ser71=
NM_018890.4:c.213C>G	NP_061485.1:p.Ser71=