Canonical Allele Identifier: CA840971663

Gene: RAC1

Linked Data

• dbSNP Id: rs376284529
• gnomAD v3: 7-6391898-C-T
• gnomAD v4: 7-6391898-C-T
• MyVariant Identifiers: chr7:g.6431529C>T (hg19) ; chr7:g.6391898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391898C>T , CM000669.2:g.6391898C>T	GRCh38
NC_000007.13:g.6431529C>T , CM000669.1:g.6431529C>T	GRCh37
NC_000007.12:g.6398054C>T	NCBI36
NG_029431.1:g.22404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.296-26C>T
ENST00000704002.1:c.207-26C>T	ENSP00000515615.1:n.207-26C>T
ENST00000704003.1:c.*61-26C>T	ENSP00000515616.1:n.*61-26C>T
ENST00000348035.9:c.108-26C>T MANE Select	ENSP00000258737.7:n.108-26C>T
ENST00000348035.8:c.108-26C>T	ENSP00000258737.7:n.108-26C>T
ENST00000356142.4:c.108-26C>T	ENSP00000348461.4:n.108-26C>T
ENST00000488373.5:n.339-26C>T
ENST00000497741.5:n.124-26C>T
NM_006908.4:c.108-26C>T	NP_008839.2:n.108-26C>T
NM_018890.3:c.108-26C>T	NP_061485.1:n.108-26C>T
NM_006908.5:c.108-26C>T MANE Select	NP_008839.2:n.108-26C>T
NM_018890.4:c.108-26C>T	NP_061485.1:n.108-26C>T