Canonical Allele Identifier: CA453648090

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431621A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391990A>C , CM000669.2:g.6391990A>C	GRCh38
NC_000007.13:g.6431621A>C , CM000669.1:g.6431621A>C	GRCh37
NC_000007.12:g.6398146A>C	NCBI36
NG_029431.1:g.22496A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.362A>C
ENST00000704002.1:c.273A>C	ENSP00000515615.1:p.Thr91=
ENST00000704003.1:c.*127A>C	ENSP00000515616.1:n.*127A>C
ENST00000348035.9:c.174A>C MANE Select	ENSP00000258737.7:p.Thr58=
ENST00000348035.8:c.174A>C	ENSP00000258737.7:p.Thr58=
ENST00000356142.4:c.174A>C	ENSP00000348461.4:p.Thr58=
ENST00000488373.5:n.405A>C
ENST00000497741.5:n.190A>C
NM_006908.4:c.174A>C	NP_008839.2:p.Thr58=
NM_018890.3:c.174A>C	NP_061485.1:p.Thr58=
NM_006908.5:c.174A>C MANE Select	NP_008839.2:p.Thr58=
NM_018890.4:c.174A>C	NP_061485.1:p.Thr58=