Canonical Allele Identifier: CA366760766
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1562466717

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.316A>G
ENST00000704002.1:c.227A>G ENSP00000515615.1:p.Asn76Ser
ENST00000704003.1:c.*81A>G ENSP00000515616.1:n.*81A>G
ENST00000348035.9:c.128A>G MANE Select ENSP00000258737.7:p.Asn43Ser
ENST00000348035.8:c.128A>G ENSP00000258737.7:p.Asn43Ser
ENST00000356142.4:c.128A>G ENSP00000348461.4:p.Asn43Ser
ENST00000488373.5:n.359A>G
ENST00000497741.5:n.144A>G
NM_006908.4:c.128A>G NP_008839.2:p.Asn43Ser
NM_018890.3:c.128A>G NP_061485.1:p.Asn43Ser
NM_006908.5:c.128A>G MANE Select NP_008839.2:p.Asn43Ser
NM_018890.4:c.128A>G NP_061485.1:p.Asn43Ser