Canonical Allele Identifier: CA153350769

Gene: RAC1

Linked Data

• dbSNP Id: rs35075100
• gnomAD v2: 7-6431927-A-G
• gnomAD v3: 7-6392296-A-G
• gnomAD v4: 7-6392296-A-G
• MyVariant Identifiers: chr7:g.6431927A>G (hg19) ; chr7:g.6392296A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392296A>G , CM000669.2:g.6392296A>G	GRCh38
NC_000007.13:g.6431927A>G , CM000669.1:g.6431927A>G	GRCh37
NC_000007.12:g.6398452A>G	NCBI36
NG_029431.1:g.22802A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.668A>G
ENST00000704002.1:c.324+255A>G	ENSP00000515615.1:n.324+255A>G
ENST00000704003.1:c.*178+255A>G	ENSP00000515616.1:n.*178+255A>G
ENST00000348035.9:c.225+255A>G MANE Select	ENSP00000258737.7:n.225+255A>G
ENST00000348035.8:c.225+255A>G	ENSP00000258737.7:n.225+255A>G
ENST00000356142.4:c.225+255A>G	ENSP00000348461.4:n.225+255A>G
ENST00000488373.5:n.456+255A>G
ENST00000497741.5:n.241+255A>G
NM_006908.4:c.225+255A>G	NP_008839.2:n.225+255A>G
NM_018890.3:c.225+255A>G	NP_061485.1:n.225+255A>G
NM_006908.5:c.225+255A>G MANE Select	NP_008839.2:n.225+255A>G
NM_018890.4:c.225+255A>G	NP_061485.1:n.225+255A>G