Canonical Allele Identifier: CA366761505

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431653C>A (hg19) ; chr7:g.6392022C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392022C>A , CM000669.2:g.6392022C>A	GRCh38
NC_000007.13:g.6431653C>A , CM000669.1:g.6431653C>A	GRCh37
NC_000007.12:g.6398178C>A	NCBI36
NG_029431.1:g.22528C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.394C>A
ENST00000704002.1:c.305C>A	ENSP00000515615.1:p.Pro102His
ENST00000704003.1:c.*159C>A	ENSP00000515616.1:n.*159C>A
ENST00000348035.9:c.206C>A MANE Select	ENSP00000258737.7:p.Pro69His
ENST00000348035.8:c.206C>A	ENSP00000258737.7:p.Pro69His
ENST00000356142.4:c.206C>A	ENSP00000348461.4:p.Pro69His
ENST00000488373.5:n.437C>A
ENST00000497741.5:n.222C>A
NM_006908.4:c.206C>A	NP_008839.2:p.Pro69His
NM_018890.3:c.206C>A	NP_061485.1:p.Pro69His
NM_006908.5:c.206C>A MANE Select	NP_008839.2:p.Pro69His
NM_018890.4:c.206C>A	NP_061485.1:p.Pro69His