Canonical Allele Identifier: CA453648203
Gene: RAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.6431639T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392008T>C , CM000669.2:g.6392008T>C GRCh38
NC_000007.13:g.6431639T>C , CM000669.1:g.6431639T>C GRCh37
NC_000007.12:g.6398164T>C NCBI36
NG_029431.1:g.22514T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.380T>C
ENST00000704002.1:c.291T>C ENSP00000515615.1:p.Tyr97=
ENST00000704003.1:c.*145T>C ENSP00000515616.1:n.*145T>C
ENST00000348035.9:c.192T>C MANE Select ENSP00000258737.7:p.Tyr64=
ENST00000348035.8:c.192T>C ENSP00000258737.7:p.Tyr64=
ENST00000356142.4:c.192T>C ENSP00000348461.4:p.Tyr64=
ENST00000488373.5:n.423T>C
ENST00000497741.5:n.208T>C
NM_006908.4:c.192T>C NP_008839.2:p.Tyr64=
NM_018890.3:c.192T>C NP_061485.1:p.Tyr64=
NM_006908.5:c.192T>C MANE Select NP_008839.2:p.Tyr64=
NM_018890.4:c.192T>C NP_061485.1:p.Tyr64=