Canonical Allele Identifier: CA840972055

Gene: RAC1

Linked Data

• dbSNP Id: rs1397572202
• gnomAD v3: 7-6392168-G-T
• gnomAD v4: 7-6392168-G-T
• MyVariant Identifiers: chr7:g.6431799G>T (hg19) ; chr7:g.6392168G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392168G>T , CM000669.2:g.6392168G>T	GRCh38
NC_000007.13:g.6431799G>T , CM000669.1:g.6431799G>T	GRCh37
NC_000007.12:g.6398324G>T	NCBI36
NG_029431.1:g.22674G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.540G>T
ENST00000704002.1:c.324+127G>T	ENSP00000515615.1:n.324+127G>T
ENST00000704003.1:c.*178+127G>T	ENSP00000515616.1:n.*178+127G>T
ENST00000348035.9:c.225+127G>T MANE Select	ENSP00000258737.7:n.225+127G>T
ENST00000348035.8:c.225+127G>T	ENSP00000258737.7:n.225+127G>T
ENST00000356142.4:c.225+127G>T	ENSP00000348461.4:n.225+127G>T
ENST00000488373.5:n.456+127G>T
ENST00000497741.5:n.241+127G>T
NM_006908.4:c.225+127G>T	NP_008839.2:n.225+127G>T
NM_018890.3:c.225+127G>T	NP_061485.1:n.225+127G>T
NM_006908.5:c.225+127G>T MANE Select	NP_008839.2:n.225+127G>T
NM_018890.4:c.225+127G>T	NP_061485.1:n.225+127G>T