Canonical Allele Identifier: CA366760961

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431602A>C (hg19) ; chr7:g.6391971A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391971A>C , CM000669.2:g.6391971A>C	GRCh38
NC_000007.13:g.6431602A>C , CM000669.1:g.6431602A>C	GRCh37
NC_000007.12:g.6398127A>C	NCBI36
NG_029431.1:g.22477A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.343A>C
ENST00000704002.1:c.254A>C	ENSP00000515615.1:p.Asn85Thr
ENST00000704003.1:c.*108A>C	ENSP00000515616.1:n.*108A>C
ENST00000348035.9:c.155A>C MANE Select	ENSP00000258737.7:p.Asn52Thr
ENST00000348035.8:c.155A>C	ENSP00000258737.7:p.Asn52Thr
ENST00000356142.4:c.155A>C	ENSP00000348461.4:p.Asn52Thr
ENST00000488373.5:n.386A>C
ENST00000497741.5:n.171A>C
NM_006908.4:c.155A>C	NP_008839.2:p.Asn52Thr
NM_018890.3:c.155A>C	NP_061485.1:p.Asn52Thr
NM_006908.5:c.155A>C MANE Select	NP_008839.2:p.Asn52Thr
NM_018890.4:c.155A>C	NP_061485.1:p.Asn52Thr