Canonical Allele Identifier: CA366760762

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431575A>C (hg19) ; chr7:g.6391944A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391944A>C , CM000669.2:g.6391944A>C	GRCh38
NC_000007.13:g.6431575A>C , CM000669.1:g.6431575A>C	GRCh37
NC_000007.12:g.6398100A>C	NCBI36
NG_029431.1:g.22450A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.316A>C
ENST00000704002.1:c.227A>C	ENSP00000515615.1:p.Asn76Thr
ENST00000704003.1:c.*81A>C	ENSP00000515616.1:n.*81A>C
ENST00000348035.9:c.128A>C MANE Select	ENSP00000258737.7:p.Asn43Thr
ENST00000348035.8:c.128A>C	ENSP00000258737.7:p.Asn43Thr
ENST00000356142.4:c.128A>C	ENSP00000348461.4:p.Asn43Thr
ENST00000488373.5:n.359A>C
ENST00000497741.5:n.144A>C
NM_006908.4:c.128A>C	NP_008839.2:p.Asn43Thr
NM_018890.3:c.128A>C	NP_061485.1:p.Asn43Thr
NM_006908.5:c.128A>C MANE Select	NP_008839.2:p.Asn43Thr
NM_018890.4:c.128A>C	NP_061485.1:p.Asn43Thr