Canonical Allele Identifier: CA453648020

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431567T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391936T>C , CM000669.2:g.6391936T>C	GRCh38
NC_000007.13:g.6431567T>C , CM000669.1:g.6431567T>C	GRCh37
NC_000007.12:g.6398092T>C	NCBI36
NG_029431.1:g.22442T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.308T>C
ENST00000704002.1:c.219T>C	ENSP00000515615.1:p.Tyr73=
ENST00000704003.1:c.*73T>C	ENSP00000515616.1:n.*73T>C
ENST00000348035.9:c.120T>C MANE Select	ENSP00000258737.7:p.Tyr40=
ENST00000348035.8:c.120T>C	ENSP00000258737.7:p.Tyr40=
ENST00000356142.4:c.120T>C	ENSP00000348461.4:p.Tyr40=
ENST00000488373.5:n.351T>C
ENST00000497741.5:n.136T>C
NM_006908.4:c.120T>C	NP_008839.2:p.Tyr40=
NM_018890.3:c.120T>C	NP_061485.1:p.Tyr40=
NM_006908.5:c.120T>C MANE Select	NP_008839.2:p.Tyr40=
NM_018890.4:c.120T>C	NP_061485.1:p.Tyr40=