Canonical Allele Identifier: CA366761628

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431665C>G (hg19) ; chr7:g.6392034C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392034C>G , CM000669.2:g.6392034C>G	GRCh38
NC_000007.13:g.6431665C>G , CM000669.1:g.6431665C>G	GRCh37
NC_000007.12:g.6398190C>G	NCBI36
NG_029431.1:g.22540C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.406C>G
ENST00000704002.1:c.317C>G	ENSP00000515615.1:p.Pro106Arg
ENST00000704003.1:c.*171C>G	ENSP00000515616.1:n.*171C>G
ENST00000348035.9:c.218C>G MANE Select	ENSP00000258737.7:p.Pro73Arg
ENST00000348035.8:c.218C>G	ENSP00000258737.7:p.Pro73Arg
ENST00000356142.4:c.218C>G	ENSP00000348461.4:p.Pro73Arg
ENST00000488373.5:n.449C>G
ENST00000497741.5:n.234C>G
NM_006908.4:c.218C>G	NP_008839.2:p.Pro73Arg
NM_018890.3:c.218C>G	NP_061485.1:p.Pro73Arg
NM_006908.5:c.218C>G MANE Select	NP_008839.2:p.Pro73Arg
NM_018890.4:c.218C>G	NP_061485.1:p.Pro73Arg